Oxa-azaspiro compounds having activity against pain

ABSTRACT

The present invention relates to oxa-azaspiro compounds having pharmacological activity towards the sigma (σ) receptor, to processes of preparation of such compounds, to pharmaceutical compositions comprising them, and to their use in therapy, in particular for the treatment of pain.

FIELD OF THE INVENTION

The present invention relates to new oxa-azaspiro compounds having affinity for sigma receptors, especially sigma-1 (σ₁) receptors, as well as to the process for the preparation thereof, to compositions comprising them, and to their use as medicaments.

BACKGROUND OF THE INVENTION

The search for new therapeutic agents has been greatly aided in recent years by better understanding of the structure of proteins and other biomolecules associated with target diseases. One important class of these proteins are the sigma (σ) receptors, cell surface receptors of the central nervous system (CNS) which may be related to the dysphoric, hallucinogenic and cardiac stimulant effects of opioids. From studies of the biology and function of sigma receptors, evidence has been presented that sigma receptor ligands may be useful in the treatment of psychosis and movement disorders such as dystonia and tardive dyskinesia, and motor disturbances associated with Huntington's chorea or Tourette's syndrome and in Parkinson's disease (Walker, J. M. et al, Pharmacological Reviews, 1990, 42, 355). It has been reported that the known sigma receptor ligand rimcazole clinically shows effects in the treatment of psychosis (Snyder, S. H., Largent, B. L. J. Neuropsychiatry 1989, 1, 7). The sigma binding sites have preferential affinity for the dextrorotatory isomers of certain opiate benzomorphans, such as (+)SKF-10047, (+)cyclazocine, and (+)-pentazocine and also for some narcoleptics such as haloperidol.

“The sigma receptor/s” as used in this application is/are well known and defined using the following citation: This binding site represents a typical protein different from opioid, NMDA, dopaminergic, and other known neurotransmitter or hormone receptor families (G. Ronsisvalle et al. Pure Appl. Chem. 73, 1499-1509 (2001)).

The sigma receptor has at least two subtypes, which may be discriminated by stereoselective isomers of these pharmacoactive drugs. (+)SKF-10047 has nanomolar affinity for the sigma-1 (σ₁) site, and has micromolar affinity for the sigma-2 (σ₂) site. Haloperidol has similar affinities for both subtypes.

The σ₁ receptor is a non-opiaceous type receptor expressed in numerous adult mammal tissues (e.g. central nervous system, ovary, testicle, placenta, adrenal gland, spleen, liver, kidney, gastrointestitestinal tract) as well as in embryo development from its earliest stages, and is apparently involved in a large number of physiological functions. Its high affinity for various pharmaceuticals has been described, such as for (+)SKF-10047, (+)-pentazocine, haloperidol and rimcazole, among others, known ligands with analgesic, anxiolytic, antidepressive, antiamnesic, antipsychotic and neuroprotective activity, σ₁ receptor is of great interest in pharmacology in view of its possible physiological role in processes related to analgesia, anxiety, addiction, amnesia, depression, schizophrenia, stress, neuroprotection and psychosis [Kaiser et al (1991) Neurotransmissions 7 (1): 1-5], [Walker, J. M. et al, Pharmacological Reviews, 1990, 42, 355] and [Bowen W. D. (2000) Pharmaceutica Acta Helvetiae 74: 211-218].

The σ₂ receptor is also expressed in numerous adult mammal tissues (e.g. nervous system, immune system, endocrine system, liver, kidney). σ₂ receptors can be components in a new apoptosis route that may play an important role in regulating cell proliferation or in cell development. This route seems to consist of σ₂ receptors joined to intracellular membranes, located in organelles storing calcium, such as the endoplasmic reticulum and mitochondria, which also have the ability to release calcium from these organelles. The calcium signals can be used in the signaling route for normal cells and/or in induction of apoptosis.

Agonists of σ₂ receptors induce changes in cell morphology, apoptosis in several types of cell lines and regulate the expression of p-glycoprotein mRNA, so that they are potentially useful as antineoplasic agents for treatment of cancer. In fact, σ₂ receptor agonists have been observed to induce apoptosis in mammary tumour cell lines resistant to common antineoplasic agents that damage DNA. In addition, agonists of σ₂ receptors enhance the cytotoxic effects of these antineoplasic agents at concentrations in which the agonist is not cytotoxic. Thus, agonists of σ₂ receptors can be used as antineoplasic agents at doses inducing apoptosis or at sub-toxic doses in combination with other antineoplasic agents to revert the resistance to the drug, thereby allowing using lower doses of the antineoplasic agent and considerably reducing its adverse effects.

Antagonists of σ₂ receptors can prevent the irreversible motor side effects caused by typical neuroleptic agents. In fact, it has been found that antagonists of σ₂ receptors can be useful as agents for improving the weakening effects of delayed dyskinesia appearing in patients due to chronic treatment of psychosis with typical antipsychotic drugs, such as haloperidol. σ₂ receptors also seem to play a role in certain degenerative disorders in which blocking these receptors could be useful.

Endogenous sigma ligands are not known, although progesterone has been suggested to be one of them. Possible sigma-site-mediated drug effects include modulation of glutamate receptor function, neurotransmitter response, neuroprotection, behavior, and cognition (Quirion, R. et al. Trends Pharmacol. Sci., 1992, 13:85-86). Most studies have implied that sigma binding sites (receptors) are plasmalemmal elements of the signal transduction cascade. Drugs reported to be selective sigma ligands have been evaluated as antipsychotics (Hanner, M. et al, Proc. Nat. Acad. Sci., 1996, 93:8072-8077). The existence of sigma receptors in the CNS, immune and endocrine systems have suggested a likelihood that it may serve as link between the three systems.

In view of the potential therapeutic applications of agonists or antagonists of the sigma receptor, a great effort has been directed to find selective ligands. Thus, the prior art discloses different sigma receptor ligands.

For instance, the international patent application WO2007/098961 describes 4,5,6,7 tetrahydrobenzo[b]thiophene derivatives having pharmacological activity towards the sigma receptor.

Spiro[benzopyran] or spiro[benzofuran] derivatives were also disclosed in EP1847542 as well as pyrazole derivatives (EP1634873) with pharmacological activity on sigma receptors.

WO20091071657 discloses some tricyclic triazolic compounds although structurally different to the ones of the current invention with activity towards sigma receptors.

Nevertheless, there is still a need to find compounds having pharmacological activity towards the sigma receptor, being both effective, selective, and/or having good “drugability” properties, i.e. good pharmaceutical properties related to administration, distribution, metabolism and excretion.

Surprisingly, it has been observed that the new oxa-azaspiro compounds with general Formula (I) show a selective affinity for σ₁ receptor ranging from good to excellent. These compounds are therefore particularly suitable as pharmacologically active agents in medicaments for the prophylaxis and/or treatment of disorders or diseases related to Sigma receptors.

SUMMARY OF THE INVENTION

The present invention discloses novel compounds with great affinity to sigma receptors and having high solubility in a physiological media which might be used for the treatment of sigma related disorders or diseases.

As this invention is aimed at providing a compound or a chemically related series of compounds which act as ligands of the σ₁ receptor it is a very preferred embodiment if the compound has a binding expressed as K_(i) which is preferably <1000 nM, more preferably <500 nM, even more preferably <100 nM.

The invention is directed in a main aspect to a compound of general Formula (I),

-   -   wherein R₁, R₂, R₃, R_(3′), R₅, R_(5′), R₆, R_(6′), R_(n), X, Y,         m and n are as defined below in the detailed description.

A further object of the invention refers to the processes for preparation of compounds of general formula (I).

A still further object of the invention refers to the use of intermediate compounds for the preparation of a compound of general formula (I).

It is also an object of the invention a pharmaceutical composition comprising a compound of formula (I).

Finally, it is an object of the invention the use of compound as a medicament and more particularly for the treatment of pain and pain related conditions.

DETAILED DESCRIPTION OF THE INVENTION

The present invention discloses novel compounds with great affinity to sigma receptors and having high solubility in a physiological media which might be used for the treatment of sigma related disorders or diseases.

As this invention is aimed at providing a compound or a chemically related series of compounds which act as ligands of the a receptor it is a very preferred embodiment if the compound has a binding expressed as K_(i) which is preferably <1000 nM, more preferably <500 nM, even more preferably <100 nM.

Advantageously, the compounds according to the present invention would in addition show one or more the following functionalities: σ₁ receptor antagonism. It has to be noted, though, that the functionalities “antagonism” and “agonism” are also sub-divided in their effect into subfunctionalities like partial agonism or inverse agonism. Accordingly, the functionalities of the compound should be considered within a relatively broad bandwidth.

An antagonist blocks or dampens agonist-mediated responses. Known subfunctionalities are neutral antagonists or inverse agonists.

An agonist increases the activity of the receptor above its basal level. Known subfunctionalities are full agonists, or partial agonists.

The invention is directed in a main aspect to a compound of general Formula (I),

In a particular aspect, the present invention is directed to compounds of general Formula (I):

wherein

R₁ is or

m is 1, 2, 3, 4 or 5; n is 0, 2, 3, 4 or 5; p is 0, 1 or 2: X is a bond, —C(R_(x)R_(x′))—, —O—, —C(O)—, —C(O)NR₇—, —NR₇C(O)— or —C(O)O—;

-   -   wherein R_(x) is selected from halogen, —OR₇, substituted or         unsubstituted C₁₋₆ alkyl, substituted or unsubstituted C₂₋₆         alkenyl and substituted or unsubstituted C₂₋₆ alkynyl;     -   R_(x′) is selected from hydrogen, halogen, substituted or         unsubstituted C₁₋₆ alkyl, substituted or unsubstituted C₂₋₆         alkenyl and substituted or unsubstituted C₂₋₆ alkynyl;     -   R₇ is selected from hydrogen, substituted or unsubstituted C₁₋₆         alkyl, substituted or unsubstituted C₂₋₆ alkenyl and substituted         or unsubstituted C₂₋₆ alkynyl;

Y is —CH₂— or —C(O)—;

R₁ is selected from substituted or unsubstituted C₁₋₆ alkyl, substituted or unsubstituted C₂₋₆ alkenyl, substituted or unsubstituted C₂₋₆ alkynyl, substituted or unsubstituted cycloalkyl, substituted or unsubstituted aryl and substituted or unsubstituted heterocyclyl: R₂ is selected from hydrogen, substituted or unsubstituted C₁₋₆ alkyl, substituted or unsubstituted C₂₋₆ alkenyl, substituted or unsubstituted C₂₋₆ alkynyl, substituted or unsubstituted cycloalkyl, substituted or unsubstituted aryl and substituted or unsubstituted heterocyclyl; R₃ and R_(3′) are independently selected from hydrogen, substituted or unsubstituted C₁₋₅ alkyl, substituted or unsubstituted C₂₋₆ alkenyl, substituted or unsubstituted C₂₋₆ alkynyl, substituted or unsubstituted cycloalkyl, substituted or unsubstituted alkylcycloalkyl, substituted or unsubstituted alkylaryl, substituted or unsubstituted aryl, substituted or unsubstituted heterocyclyl or substituted or unsubstituted alkylheterocyclyl; alternatively R₃ and R_(3′) taken together with the connecting C-atom may form an substituted or unsubstituted cycloalkyl; R₄ and R_(4′) are independently selected from hydrogen, substituted or unsubstituted C₁₋₆ alkyl, substituted or unsubstituted C₂₋₆ alkenyl and substituted or unsubstituted C₂₋₆ alkynyl; R₅ and R_(5′) are independently selected from hydrogen, substituted or unsubstituted C₁₋₆ alkyl, substituted or unsubstituted C₂₋₆ alkenyl, substituted or unsubstituted C₂₋₆ alkynyl, substituted or unsubstituted cycloalkyl and substituted or unsubstituted heterocyclyl; alternatively, R₅ and R_(5′) taken together with the connecting C-atom may form an substituted or unsubstituted cycloalkyl or a substituted or unsubstituted heterocyclyl; R₆ and R_(6′) are independently selected from hydrogen, halogen, substituted or unsubstituted C₁₋₆ alkyl, substituted or unsubstituted C₂₋₆ alkenyl, substituted or unsubstituted C₂₋₆ alkynyl, —CHOR₈ and —C(O)OR₈:

-   -   wherein R₈ is selected from hydrogen, substituted or         unsubstituted C₁₋₆ alkyl, substituted or unsubstituted C₂₋₆         alkenyl and substituted or unsubstituted C₂₋₆ alkynyl;         R_(n) is selected from hydrogen, unsubstituted C₁₋₆ alkyl,         unsubstituted C₂₋₆ alkenyl and unsubstituted C₂₋₆ alkynyl;

These compounds according to the invention are optionally in form of one of the stereoisomers, preferably enantiomers or diastereomers, a racemate or in form of a mixture of at least two of the stereoisomers, preferably enantiomers and/or diastereomers, in any mixing ratio, or a corresponding salt thereof, or a corresponding solvate thereof.

Thus, the compounds according to Formula (I) may take for example the following sterochemical conformation:

In a further embodiment the following proviso applies:

when Y is-C(O)—; then R₁ is not

In a further embodiment the compound according to the invention of general Formula (I) is a compound of general Formula (I′)

wherein, R₁, R₂, R₃, R_(3′), R₅, R_(5′), R_(n), Y and m are as defined in the description.

In a further embodiment the compound according to the invention of general Formula (I) is a compound of general Formula (I^(a′))

wherein, R₁, R₂, R₅, R_(5′), R_(n), Y and m are as defined in the description.

In a further embodiment the compound according to the invention of general Formula (I) is a compound of general Formula (I^(b′))

wherein, R₁, R₂, R₅, R_(5′), R_(n), Y and m are as defined in the description.

In a further embodiment the compound according to the invention of general Formula (I) is a compound of general Formula (I^(2′))

wherein R₁, R₂, R₅, R_(5′), R_(n), Y and m are as defined in the description.

In a further embodiment, for compounds of general Formula (I) are compounds of general Formula (I^(3′))

wherein R_(1′), R₂, R₅, R_(5′), R_(n), Y and m are as defined in the description.

For clarity purposes, reference is also made to the following statements below in the definitions of substitutions on alkyl etc. or aryl etc. that “wherein when different radicals R₁ to R_(14″″) and R_(x), R_(x′) and R_(n) are present simultaneously in Formula I they may be identical or different”. This statement is reflected in the below general Formula (I^(4′)) being derived from and falling into general Formula (I).

wherein R₁, R₂, R₅, R_(5′), R_(n), X and Y are as defined in the description. In addition, m′ (being 0 or 1), R_(5″) and R_(5′″) are added. As said above, this statement is thus reflected in that R_(5″) and R_(5′″) are or could be different from R₅ and R_(5′) or not and—accordingly—m′ being 0 or 1 is naturally resulting from m (in general Formulas (I), (I), (I^(a′)), (I^(b′)), (I^(2′)) or (I^(3′)) being 1 or 2).

The same would be applicable mutatis mutandis for general Formulas like general Formula (I) as well as the other general Formulas (I) to (I^(3′)) above as well as to all the intermediates of synthesis.

For clarity purposes, all groups and definitions described in the description and referring to compounds of general Formula (I), also apply to compounds of general Formula (I), (I^(a′)), (I^(b′)), (I^(2′)) or (I^(3′)), and also (I^(4′)), as well as to all the intermediates of synthesis, when those groups are present in the mentioned general Markush formulae, since compounds of general Formula (I′), (I^(a′)), (I^(b′)), (I^(2′)), (I^(3′)) or (I^(4′)) are included in the general Formula (I).

For clarity purposes, the general Markush Formula (I)

is equivalent to

wherein only —C(R₅R_(5′))— and —C(R₆R_(6′))— are included into the brackets and m and n mean the number of times that —C(R₅R_(5′))— and —C(R₆R_(6′))— are repeated, respectively. The same would apply to general Markush Formulae (I′), (I^(a′)), (I^(b′)), (I^(2′)), (I^(3′)) or (I^(4′)) and to all the intermediates of synthesis.

In addition, and for clarity purposes, it should further be understood that naturally if m or n are 0, then X, —N(R_(n))— or R₂ are still present in general Markush Formulae (I), (I′), (I^(a′)), (I^(b′)), (I^(2′)), (I^(3′)) or (I^(4′)) and to all the intermediates of synthesis.

In the context of this invention, alkyl is understood as meaning saturated, linear or branched hydrocarbons, which may be unsubstituted or substituted once or several times. It encompasses e.g. —CH₃ and —CH₂—CH₃. In these radicals, C₁₋₂-alkyl represents C1- or C2-alkyl, C₁₋₃-alkyl represents C1-, C2- or C3-alkyl, C₁₋₄-alkyl represents C1-, C2-, C3- or C4-alkyl, C₁₋₅-alkyl represents C1-, C2-, C3-, C4-, or C₅-alkyl, C₁₋₆-alkyl represents C1-, C2-, C3-, C4-, C5- or C6-alkyl, C₁₋₇-alkyl represents C1-, C2-, C3-, C4-, C5-, C6- or C7-alkyl, C₁₋₈-alkyl represents C1-, C2-, C3-, C4-, C5-, C6-, C7- or C8-alkyl, C₁₋₁₀-alkyl represents C1-, C2-, C3-, C4-, C5-, C6-, C7-, C8-, C9- or C10-alkyl and C₁₋₁₈-alkyl represents C1-, C2-, C3-, C4-, C5-, C6-, C7-, C8-, C9-, C10-, C11-, C12-, C13-, C14-, C15-, C16-, C17- or C18-alkyl. The alkyl radicals are preferably methyl, ethyl, propyl, methylethyl, butyl, 1-methylpropyl, 2-methylpropyl, 1,1-dimethylethyl, pentyl, 1,1-dimethylpropyl, 1,2-dimethylpropyl, 2,2-dimethylpropyl, hexyl, 1-methylpentyl, if substituted also CHF₂, CF₃ or CH₂OH etc. Preferably alkyl is understood in the context of this invention as C₁₋₈alkyl like methyl, ethyl, propyl, butyl, pentyl, hexyl, heptyl, or octyl; preferably is C₁₋₆alkyl like methyl, ethyl, propyl, butyl, pentyl, or hexyl; more preferably is C₁₋₄alkyl like methyl, ethyl, propyl or butyl.

Alkenyl is understood as meaning unsaturated, linear or branched hydrocarbons, which may be unsubstituted or substituted once or several times. It encompasses groups like e.g. —CH═CH—CH₃. The alkenyl radicals are preferably vinyl (ethenyl), allyl (2-propenyl). Preferably in the context of this invention alkenyl is C₂₋₁₀-alkenyl or C₂₋₈-alkenyl like ethylene, propylene, butylene, pentylene, hexylene, heptylene or octylene; or is C₂₋₆-alkenyl like ethylene, propylene, butylene, pentylene, or hexylene; or is C₂₋₄-alkenyl, like ethylene, propylene, or butylenes.

Alkynyl is understood as meaning unsaturated, linear or branched hydrocarbons, which may be unsubstituted or substituted once or several times. It encompasses groups like e.g. —C═C—CH₃ (1-propinyl). Preferably alkynyl in the context of this invention is C₂₋₁₀-alkynyl or C₂₋₈-alkynyl like ethyne, propyne, butyene, pentyne, hexyne, heptyne, or octyne; or is C₂₋₆-alkynyl like ethyne, propyne, butyene, pentyne, or hexyne; or is C₂₋₄-alkynyl like ethyne, propyne, butyene, pentyne, or hexyne.

In connection with alkyl (also in alkylaryl, alkylheterocyclyl or alkylcycloalkyl), alkenyl, alkynyl and O-alkyl—unless defined otherwise—the term substituted in the context of this invention is understood as meaning replacement of at least one hydrogen radical on a carbon atom by halogen (F, Cl, Br, I), —NR_(c)R_(c′″), —SR_(c), —S(O)R_(c), —S(O)₂R_(c), —OR_(c), —C(O)OR_(c), —CN, —C(O)NR_(c)R_(c′), haloalkyl, haloalkoxy or —OC₁₋₆ alkyl being R_(c) represented by R₁₁, R₁₂, R₁₃, (being R_(c′) represented by R_(11′), R_(12′), R_(13′); being R_(c″) represented by R_(11″), R_(12″), R_(13″); being R_(c′″) represented by R_(11′″), R_(12′″), R_(13′″), being R_(c″″) represented by R_(11″″), R_(12″″), R_(13″″)) wherein R₁ to R_(14″″) and R_(x), R_(x′) and R_(n) are as defined in the description, and wherein when different radicals R₁ to R_(14″″) and R_(x), R_(x′) and R_(n) are present simultaneously in Formula I they may be identical or different.

Most preferably in connection with alkyl (also in alkylaryl, alkylheterocyclyl or alkylcycloalkyl), alkenyl, alkynyl or O-alkyl, substituted is understood in the context of this invention that any alkyl (also in alkylaryl, alkylheterocyclyl or alkylcycloalkyl), alkenyl, alkynyl or O-alkyl which is substituted is substituted with one or more of halogen (F, Cl, Br, I), —OR_(c), —CN, —NR_(c)R_(c′″), haloalkyl, haloalkoxy or —OC₁₋₆alkyl, being R_(c) represented by R₁₁, R₁₂, R₁₃, (being R_(c′) represented by R_(11′), R_(12′), R_(13′); being R_(c″) represented by R_(11″), R_(12″), R_(13″); being R_(c′″) represented by R_(11′″), R_(12′″), R_(13′″), being R_(c″″), represented by R_(11″″), R_(12″″), R_(13″″)), wherein R₁ to R_(14″″) and R_(x), R_(x′) and R_(n) are as defined in the description, and wherein when different radicals R₁ to R_(14″″) and R_(x), R_(x′) and R_(n) are present simultaneously in Formula I, they may be identical or different.

More than one replacement on the same molecule and also on the same carbon atom is possible with the same or different substituents. This includes for example 3 hydrogens being replaced on the same C atom, as in the case of CF₃, or at different places of the same molecule, as in the case of e.g. —CH(OH)—CH═CH—CHCl₂.

In the context of this invention haloalkyl is understood as meaning an alkyl being substituted once or several times by a halogen (selected from F, Cl, Br, I). It encompasses e.g. —CH₂Cl, —CH₂F, —CHCl₂, —CHF₂, —CCl₃, —CF₃ and —CH₂—CHCl₂. Preferably haloalkyl is understood in the context of this invention as halogen-substituted C₁₋₄-alkyl representing halogen substituted C1-, C2-, C3- or C4-alkyl. The halogen-substituted alkyl radicals are thus preferably methyl, ethyl, propyl, and butyl. Preferred examples include —CH₂Cl, —CH₂F, —CHCl₂, —CHF₂, and —CF₃.

In the context of this invention haloalkoxy is understood as meaning an —O-alkyl being substituted once or several times by a halogen (selected from F, Cl, Br, I). It encompasses e.g. —OCH₂Cl, —OCH₂F, —OCHCl₂, —OCHF₂, —OCCl₃, —OCF₃ and —OCH₂—CHCl₂. Preferably haloalkyl is understood in the context of this invention as halogen-substituted —OC₁₋₄-alkyl representing halogen substituted C1-, C2-, C3- or C4-alkoxy. The halogen-substituted alkyl radicals are thus preferably O-methyl, O-ethyl, O-propyl, and O-butyl. Preferred examples include —OCH₂Cl, —OCH₂F, —OCHCl₂, —OCHF₂, and —OCF₃.

In the context of this invention cycloalkyl is understood as meaning saturated and unsaturated (but not aromatic) cyclic hydrocarbons (without a heteroatom in the ring), which can be unsubstituted or once or several times substituted. Furthermore, C₃₋₄-cycloalkyl represents C3- or C4-cycloalkyl, C₃₋₅-cycloalkyl represents C3-, C4- or C5-cycloalkyl, C₃₋₆-cycloalkyl represents C3-, C4-, C5- or C6-cycloalkyl, C₃₋₇-cycloalkyl represents C3-, C4-, C5-, C6- or C7-cycloalkyl, C₃₋₈-cycloalkyl represents C3-, C4-, C5-, C6-, C7- or C8-cycloalkyl, C₄₋₅-cycloalkyl represents C4- or C5-cycloalkyl, C₄₋₆-cycloalkyl represents C4-, C5- or C6-cycloalkyl, C₄₋₇-cycloalkyl represents C4-, C5-, C6- or C7-cycloalkyl, C₅₋₆-cycloalkyl represents C5- or C6-cycloalkyl and C₅₋₇-cycloalkyl represents C5-, C6- or C7-cycloalkyl. Examples are cyclopropyl, 2-methylcyclopropyl, cyclopropylmethyl, cyclobutyl, cyclopentyl, cyclopentylmethyl, cyclohexyl, cycloheptyl, cyclooctyl, and also adamantly. Preferably in the context of this invention cycloalkyl is C₃₋₈cycloalkyl like cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, cycloheptyl, or cyclooctyl; or is C₃₋₇cycloalkyl like cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, or cycloheptyl; or is C₃₋₆cycloalkyl like cyclopropyl, cyclobutyl, cyclopentyl or cyclohexyl, especially cyclopentyl or cyclohexyl.

Aryl is understood as meaning 5 to 18 membered mono or polycyclic ring systems with at least one aromatic ring but without heteroatoms even in only one of the rings. Examples are phenyl, naphthyl, fluoranthenyl, fluorenyl, tetralinyl or indany, 9H-fluorenyl or anthracenyl radicals, which can be unsubstituted or once or several times substituted. Most preferably aryl is understood in the context of this invention as phenyl, naphtyl or anthracenyl, preferably is phenyl.

A heterocyclyl radical or group (also called heterocyclyl hereinafter) is understood as meaning 5 to 18 membered mono or polycyclic heterocyclic ring systems, with at least one saturated or unsaturated ring which contains one or more heteroatoms from the group consisting of nitrogen, oxygen and/or sulfur in the ring. A heterocyclic group can also be substituted once or several times.

Examples include non-aromatic heterocyclyls such as tetrahydropyrane, oxazepane, morpholine, piperidine, pyrrolidine as well as heteroaryls such as furan, benzofuran, thiophene, benzothiophene, pyrrole, pyridine, pyrimidine, pyrazine, quinoline, isoquinoline, phthalazine, thiazole, benzothiazole, indole, benzotriazole, carbazole and quinazoline.

Subgroups inside the heterocyclyls as understood herein include heteroaryls and non-aromatic heterocyclyls.

-   -   the heteroaryl (being equivalent to heteroaromatic radicals or         aromatic heterocyclyls) is an aromatic 5 to 18 membered mono or         polycyclic heterocyclic ring system of one or more rings of         which at least one aromatic ring contains one or more         heteroatoms from the group consisting of nitrogen, oxygen and/or         sulfur in the ring; preferably is an aromatic 5 to 18 membered         mono or polycyclic heterocyclic ring system of one or two rings         of which at least one aromatic ring contains one or more         heteroatoms from the group consisting of nitrogen, oxygen and/or         sulfur in the ring, more preferably is selected from furan,         benzofuran, thiophene, benzothiophene, pyrrole, pyridine,         pyrimidine, pyrazine, quinoline, isoquinoline, phthalazine,         benzothiazole, indole, benzotriazole, carbazole, quinazoline,         thiazole, imidazole, pyrazole, oxazole, thiophene and         benzimidazole;     -   the non-aromatic heterocyclyl is a 5 to 18 membered mono or         polycyclic heterocyclic ring system of one or more rings of         which at least one ring—with this (or these) ring(s) then not         being aromatic—contains one or more heteroatoms from the group         consisting of nitrogen, oxygen and/or sulfur in the ring;         preferably is a 5 to 18 membered mono or polycyclic heterocyclic         ring system of one or two rings of which one or both rings—with         this one or two rings then not being aromatic—contain/s one or         more heteroatoms from the group consisting of nitrogen, oxygen         and/or sulfur in the ring, more preferably is selected from         oxazepam, pyrrolidine, piperidine, piperazine, tetrahydropyran,         morpholine, indoline, oxopyrrolidine, benzodioxane, oxetane,         especially is benzodioxane, morpholine, tetrahydropyran,         piperidine, oxopyrrolidine, oxetane and pyrrolidine.

Preferably in the context of this invention heterocyclyl is defined as a 5 to 18 membered mono or polycyclic heterocyclic ring system of one or more saturated or unsaturated rings of which at least one ring contains one or more heteroatoms from the group consisting of nitrogen, oxygen and/or sulfur in the ring. Preferably it is a 5 to 18 membered mono or polycyclic heterocyclic ring system of one or two saturated or unsaturated rings of which at least one ring contains one or more heteroatoms from the group consisting of nitrogen, oxygen and/or sulfur in the ring.

Preferred examples of heterocyclyls include oxetane, oxazepane, pyrrolidine, imidazole, oxadiazole, tetrazole, pyridine, pyrimidine, piperidine, piperazine, benzofuran, benzimidazole, indazole, benzodiazole, thiazole, benzothiazole, tetrahydropyrane, morpholine, indoline, furan, triazole, isoxazole, pyrazole, thiophene, benzothiophene, pyrrole, pyrazine, pyrrolo[2,3b]pyridine, quinoline, isoquinoline, phthalazine, benzo-1,2,5-thiadiazole, indole, benzotriazole, benzoxazole oxopyrrolidine, pyrimidine, benzodioxolane, benzodioxane, carbazole and quinazoline, especially is pyridine, pyrazine, indazole, benzodioxane, thiazole, benzothiazole, morpholine, tetrahydropyrane, pyrazole, imidazole, piperidine, thiophene, indole, benzimidazole, pyrrolo[2,3b]pyridine, benzoxazole, oxopyrrolidine, pyrimidine, oxazepane, oxetane and pyrrolidine.

In the context of this invention oxopyrrolidine is understood as meaning pyrrolidin-2-one.

In connection with aromatic heterocyclyls (heteroaryls), non-aromatic heterocyclyls, aryls and cycloalkyls, when a ring system falls within two or more of the above cycle definitions simultaneously, then the ring system is defined first as an aromatic heterocyclyl (heteroaryl) if at least one aromatic ring contains a heteroatom. If no aromatic ring contains a heteroatom, then the ring system is defined as a non-aromatic heterocyclyl if at least one non-aromatic ring contains a heteroatom. If no non-aromatic ring contains a heteroatom, then the ring system is defined as an aryl if it contains at least one aryl cycle. If no aryl is present, then the ring system is defined as a cycloalkyl if at least one non-aromatic cyclic hydrocarbon is present.

In the context of this invention alkylaryl is understood as meaning an aryl group (see above) being connected to another atom through a C₁₋₆-alkyl (see above) which may be branched or linear and is unsubstituted or substituted once or several times. Preferably alkylaryl is understood as meaning an aryl group (see above) being connected to another atom through 1 to 4 (—CH₂—) groups. Most preferably alkylaryl is benzyl (i.e. —CH₂-phenyl).

In the context of this invention alkylheterocyclyl is understood as meaning an heterocyclyl group being connected to another atom through a C₁₋₆-alkyl (see above) which may be branched or linear and is unsubstituted or substituted once or several times. Preferably alkylheterocyclyl is understood as meaning an heterocyclyl group (see above) being connected to another atom through 1 to 4 (—CH₂—) groups. Most preferably alkylheterocyclyl is —CH₂-pyridine.

In the context of this invention alkylcycloalkyl is understood as meaning an cycloalkyl group being connected to another atom through a C₁₋₆-alkyl (see above) which may be branched or linear and is unsubstituted or substituted once or several times. Preferably alkylcycloalkyl is understood as meaning an cycloalkyl group (see above) being connected to another atom through 1 to 4 (—CH₂—) groups. Most preferably alkylcycloalkyl is —CH₂-cyclopropyl.

Preferably, the aryl is a monocyclic aryl. More preferably the aryl is a 5, 6 or 7 membered monocyclic aryl. Even more preferably the aryl is a 5 or 6 membered monocyclic aryl.

Preferably, the heteroaryl is a monocyclic heteroaryl. More preferably the heteroaryl is a 5, 6 or 7 membered monocyclic heteroaryl. Even more preferably the heteroaryl is a 5 or 6 membered monocyclic heteroaryl.

Preferably, the non-aromatic heterocyclyl is a monocyclic non-aromatic heterocyclyl. More preferably the non-aromatic heterocyclyl is a 4, 5, 6 or 7 membered monocyclic non-aromatic heterocyclyl. Even more preferably the non-aromatic heterocyclyl is a 5 or 6 membered monocyclic non-aromatic heterocyclyl.

Preferably, the cycloalkyl is a monocyclic cycloalkyl. More preferably the cycloalkyl is a 3, 4, 5, 6, 7 or 8 membered monocyclic cycloalkyl. Even more preferably the cycloalkyl is a 3, 4, 5 or 6 membered monocyclic cycloalkyl.

In connection with aryl (including alkyl-aryl), cycloalkyl (including alkyl-cycloalkyl), or heterocyclyl (including alkyl-heterocyclyl), substituted is understood—unless defined otherwise—as meaning substitution of the ring-system of the aryl or alkyl-aryl, cycloalkyl or alkyl-cycloalkyl; heterocyclyl or alkyl-heterocyclyl with one or more of halogen (F, Cl, Br, I), —R_(c), —OR_(c), —CN, —NO₂, —NR_(c)NR_(c′″), —C(O)R_(c), NR_(c)C(O)R_(c′), —C(O)NR_(c)R_(c′), —NR_(c)S(O)₂R_(c′), ═O, —OCH₂CH₂OH, —NR_(c)C(O)NR_(c′)R_(c″), —S(O)₂NR_(c)R_(c′), —NR_(c)S(O)₂NR_(c′)R_(c″), haloalkyl, haloalkoxy, —SR_(c), —S(O)R_(c), —S(O)₂R_(c) or C(CH₃)OR_(c); NR_(c)R_(c′″), with R_(c), R_(c′), R_(c″) and R_(c′″) independently being either H or a saturated or unsaturated, linear or branched, substituted or unsubstituted C₁₋₆alkyl; a saturated or unsaturated, linear or branched, substituted or unsubstituted C₁₋₆-alkyl; a saturated or unsaturated, linear or branched, substituted or unsubstituted —O—C₁₋₆-alkyl (alkoxy); a saturated or unsaturated, linear or branched, substituted or unsubstituted —S—C₁₋₆alkyl; a saturated or unsaturated, linear or branched, substituted or unsubstituted —C(O)—C₁₋₆-alkyl-group; a saturated or unsaturated, linear or branched, substituted or unsubstituted —C(O)—O—C₁₋₆-alkyl-group; a substituted or unsubstituted aryl or alkyl-aryl; a substituted or unsubstituted cycloalkyl or alkyl-cycloalkyl; a substituted or unsubstituted heterocyclyl or alkyl-heterocyclyl, being R_(c) one of R₁₁, R₁₂ or R₁₄, (being R_(c′) one of R_(11′), R_(12′) or R_(14′); being R_(c″) one of R_(11″), R_(12″) or R_(14″); being R_(c′″) one of R_(11′″), R_(12′″) or R_(14′″); being R_(c″″) one of R_(11″″), R_(12″″) or R_(14″″)) wherein R₁ to R_(14″″) and R_(x), R_(x′) and R_(n) are as defined in the description, and wherein when different radicals R₁ to R_(14″″) and R_(x), R_(x′) and R_(n) are present simultaneously in Formula I they may be identical or different.

Most preferably in connection with aryl (including alkyl-aryl), cycloalkyl (including alkyl-cycloalkyl), or heterocyclyl (including alkyl-heterocyclyl), substituted is understood in the context of this invention that any aryl, cycloalkyl and heterocyclyl which is substituted is substituted (also in an alyklaryl, alkylcycloalkyl or alkylheterocyclyl) with one or more of halogen (F, Cl, Br, I), —R_(c), —OR_(c), —CN, —NO₂, —NR_(c)R_(c′″), NR_(c)C(O)R_(c′), —NR_(c)S(O)₂R_(c′), ═O, haloalkyl, haloalkoxy, or C(CH₃)OR_(c); —OC₁₋₄alkyl being unsubstituted or substituted with one or more of OR_(c) or halogen (F, Cl, I, Br), —CN, or —C₁₋₄alkyl being unsubstituted or substituted with one or more of OR_(c) or halogen (F, Cl, I, Br), being R_(c) one of R₁₁, R₁₂ or R₁₄, (being R_(c′) one of R_(11′), R_(12′) or R_(14′); being R_(c″) one of R_(11″), R₁₂″ or R_(14″); being R_(c′″) one of R_(11′″), R_(12′″) or R_(14′″); being R_(c″″) one of R_(11″″), R_(12″″) or R_(14″″)), wherein R₁ to R_(14″″) and R_(x), R_(x′) and R_(n) are as defined in the description, and wherein when different radicals R₁ to R_(14″″) and R_(x), R_(x′), and R_(n) are present simultaneously in Formula I they may be identical or different.

Additionally to the above-mentioned substitutions, in connection with cycloalkyl (including alkyl-cycloalkyl), or heterocycly (including alkylheterocyclyl) namely non-aromatic heterocyclyl (including non-aromatic alkyl-heterocyclyl), substituted is also understood—unless defined otherwise—as meaning substitution of the ring-system of the cycloalkyl or alkyl-cycloalkyl; non-aromatic heterocyclyl or non aromatic alkyl-heterocyclyl with

or ═O.

A ring system is a system consisting of at least one ring of connected atoms but including also systems in which two or more rings of connected atoms are joined with “joined” meaning that the respective rings are sharing one (like a spiro structure), two or more atoms being a member or members of both joined rings.

The term “leaving group” means a molecular fragment that departs with a pair of electrons in heterolytic bond cleavage. Leaving groups can be anions or neutral molecules. Common anionic leaving groups are halides such as Cl—, Br—, and I—, and sulfonate esters, such as tosylate (TsO—) or mesylate.

The term “salt” is to be understood as meaning any form of the active compound used according to the invention in which it assumes an ionic form or is charged and is coupled with a counter-ion (a cation or anion) or is in solution. By this are also to be understood complexes of the active compound with other molecules and ions, in particular complexes via ionic interactions.

The term “physiologically acceptable salt” means in the context of this invention any salt that is physiologically tolerated (most of the time meaning not being toxic—especially not caused by the counter-ion) if used appropriately for a treatment especially if used on or applied to humans and/or mammals.

These physiologically acceptable salts can be formed with cations or bases and in the context of this invention is understood as meaning salts of at least one of the compounds used according to the invention—usually a (deprotonated) acid—as an anion with at least one, preferably inorganic, cation which is physiologically tolerated—especially if used on humans and/or mammals. The salts of the alkali metals and alkaline earth metals are particularly preferred, and also those with NH₄, but in particular (mono)- or (di)sodium, (mono)- or (di)potassium, magnesium or calcium salts.

Physiologically acceptable salts can also be formed with anions or acids and in the context of this invention is understood as meaning salts of at least one of the compounds used according to the invention as the cation with at least one anion which are physiologically tolerated—especially if used on humans and/or mammals. By this is understood in particular, in the context of this invention, the salt formed with a physiologically tolerated acid, that is to say salts of the particular active compound with inorganic or organic acids which are physiologically tolerated—especially if used on humans and/or mammals. Examples of physiologically tolerated salts of particular acids are salts of: hydrochloric acid, hydrobromic acid, sulfuric acid, methanesulfonic acid, formic acid, acetic acid, oxalic acid, succinic acid, malic acid, tartaric acid, mandelic acid, fumaric acid, lactic acid or citric acid.

The compounds of the invention may be present in crystalline form or in the form of free compounds like a free base or acid.

Any compound that is a solvate of a compound according to the invention like a compound according to general formula I defined above is understood to be also covered by the scope of the invention. Methods of solvation are generally known within the art. Suitable solvates are pharmaceutically acceptable solvates. The term “solvate” according to this invention, is to be understood as meaning any form of the active compound according to the invention in which this compound has attached to it via non-covalent binding another molecule (most likely a polar solvent). Especially preferred examples include hydrates and alcoholates, like methanolates or ethanolates.

Any compound that is a prodrug of a compound according to the invention like a compound according to general formula I defined above is understood to be also covered by the scope of the invention. The term “prodrug” is used in its broadest sense and encompasses those derivatives that are converted in vivo to the compounds of the invention. Such derivatives would readily occur to those skilled in the art, and include, depending on the functional groups present in the molecule and without limitation, the following derivatives of the present compounds: esters, amino acid esters, phosphate esters, metal salts sulfonate esters, carbamates, and amides. Examples of well known methods of producing a prodrug of a given acting compound are known to those skilled in the art and can be found e.g. in Krogsgaard-Larsen et al. “Textbook of Drug design and Discovery” Taylor & Francis (April 2002).

Any compound that is a N-oxide of a compound according to the invention like a compound according to general formula I defined above is understood to be also covered by the scope of the invention.

Unless otherwise stated, the compounds of the invention are also meant to include compounds which differ only in the presence of one or more isotopically enriched atoms. For example, compounds having the present structures except for the replacement of a hydrogen by a deuterium or tritium, or the replacement of a carbon by ¹³C- or ¹⁴C-enriched carbon or of a nitrogen by ¹⁵N-enriched nitrogen are within the scope of this invention.

The compounds of formula (I) as well as their salts or solvates of the compounds are preferably in pharmaceutically acceptable or substantially pure form. By pharmaceutically acceptable form is meant, inter alia, having a pharmaceutically acceptable level of purity excluding normal pharmaceutical additives such as diluents and carriers, and including no material considered toxic at normal dosage levels. Purity levels for the drug substance are preferably above 50%, more preferably above 70%, most preferably above 90%. In a preferred embodiment it is above 95% of the compound of formula (I), or of its salts. This applies also to its solvates or prodrugs.

In a further embodiment the compound according to the invention of general Formula (I)

is a compound wherein

R₁ is

m is 1, 2, 3, 4 or 5; n is 0, 1, 2, 3, 4 or 5; p is 0, 1 or 2; X is a bond, —C(R_(x)R_(x′))—, —O—, —C(O)—, —C(O)NR₇—, —NR₇C(O)— or —C(O)O—;

-   -   wherein R_(x) is selected from halogen, —OR₇, substituted or         unsubstituted C₁₋₆ alkyl, substituted or unsubstituted C₂₋₆         alkenyl and substituted or unsubstituted C₂₋₆ alkynyl;     -   R_(x′) is selected from hydrogen, halogen, substituted or         unsubstituted C₁₋₆ alkyl, substituted or unsubstituted C₂₋₆         alkenyl and substituted or unsubstituted C₂₋₆ alkynyl;     -   R₇ is selected from hydrogen, substituted or unsubstituted C₁₋₆         alkyl, substituted or unsubstituted C₂₋₆ alkenyl and substituted         or unsubstituted C₂₋₆ alkynyl;

Y is —CH— or —C(O)—;

R_(1′) is selected from substituted or unsubstituted C₁₋₆ alkyl, substituted or unsubstituted C₂₋₆ alkenyl, substituted or unsubstituted C₂₋₆ alkynyl, substituted or unsubstituted cycloalkyl, substituted or unsubstituted aryl and substituted or unsubstituted heterocyclyl;

-   -   wherein said cycloalkyl, aryl or heterocyclyl in R_(1′) if         substituted, is substituted with one or more substituent/s         selected from halogen, —R₁₁, —OR₁₁, —NO₂, —NR₁₁R_(11′″),         NR₁₁C(O)R_(11′), —NR₁₁S(O)₂R₁₁, —S(O)₂NR₁₁R_(11′),         —NR₁₁C(O)NR_(11′)R_(11″), —SR₁₁, —S(O)R₁₁, S(O)₂R₁₁, —CN,         haloalkyl, haloalkoxy, —C(O)OR₁₁, —C(O)NR₁₁R_(11′), —OCH₂CH₂OH,         —NR₁₁S(O)₂NR_(11′)R_(11″) and C(CH₃)₂OR₁₁;     -   additionally, cycloalkyl or non-aromatic heterocyclyl in R_(1′),         if substituted, may also be substituted with

or ═O;

-   -   wherein the alkyl, alkenyl or alkynyl in R_(1′), if substituted,         is substituted with one or more substituent/s selected from         —OR₁₁, halogen, —CN, haloalkyl, haloalkoxy and —NR₁₁R_(11′″);     -   wherein R₁₁, R_(11′) and R_(11″) are independently selected from         hydrogen, unsubstituted C₁₋₆ alkyl, unsubstituted C₂₋₆ alkenyl         and unsubstituted C₂₋₆ alkynyl;     -   and wherein R_(11′″) is selected from hydrogen, unsubstituted         C₁₋₆ alkyl, unsubstituted C₂₋₆ alkenyl, unsubstituted C₂₋₆         alkynyl and -Boc;         R₂ is selected from hydrogen, substituted or unsubstituted C₁₋₆         alkyl, substituted or unsubstituted C₂₋₆ alkenyl, substituted or         unsubstituted C₂₋₆ alkynyl, substituted or unsubstituted         cycloalkyl, substituted or unsubstituted aryl and substituted or         unsubstituted heterocyclyl;     -   wherein said cycloalkyl, aryl or heterocyclyl in R₂, if         substituted, is substituted with one or more substituent/s         selected from halogen, —R₁₂, —OR₁₂, —NO₂, —NR₁₂R_(12′″),         NR₂C(O)R_(12′), —NR₁₂S(O)₂R_(21′), —S(O)₂NR₁₂R_(12′),         —NR₁₂C(O)NR_(12′)R_(12″), —SR₁₂, —S(O)R₁₂, S(O)₂R₁₂, —CN,         haloalkyl, haloalkoxy, —C(O)OR₁₂, —C(O)NR₁₂R₁₂, —OCH₂CH₂OH,         —NR₁₂S(O)₂NR_(12′)R_(12″) and C(CH₃)₂OR₁₂;     -   additionally, cycloalkyl or non-aromatic heterocyclyl in R₂, if         substituted, may also be substituted with

or ═O;

-   -   wherein the alkyl, alkenyl or alkynyl in R₂, if substituted, is         substituted with one or more substituent/s selected from —OR₁₂,         halogen, —CN, haloalkyl, haloalkoxy and —NR₁₂R_(12′″);     -   wherein R₁₂, R_(12′) and R_(12″) are independently selected from         hydrogen, unsubstituted C₁₋₆ alkyl, unsubstituted C₂₋₆ alkenyl         and unsubstituted C₂₋₆ alkynyl;     -   and wherein R_(12′″) is selected from hydrogen, unsubstituted         C₁₋₆ alkyl, unsubstituted C₂₋₆ alkenyl, unsubstituted C₂₋₆         alkynyl and -Boc;         R₃ and R_(3′) are independently selected from hydrogen,         substituted or unsubstituted C₁₋₆ alkyl, substituted or         unsubstituted C₂₋₆ alkenyl, substituted or unsubstituted C₂₋₆         alkynyl, substituted or unsubstituted cycloalkyl, substituted or         unsubstituted alkylcycloalkyl, substituted or unsubstituted         alkylaryl, substituted or unsubstituted aryl, substituted or         unsubstituted heterocyclyl or substituted or unsubstituted         alkylheterocyclyl;         alternatively R₃ and R_(3′) taken together with the connecting         C-atom may form an substituted or unsubstituted cycloalkyl;         R₄ and R_(4′) are independently selected from hydrogen,         substituted or unsubstituted C₁₋₆ alkyl, substituted or         unsubstituted C₂₋₆ alkenyl and substituted or unsubstituted C₂₋₆         alkynyl;         R₅ and R_(5′) are independently selected from hydrogen,         substituted or unsubstituted C₁₋₆ alkyl, substituted or         unsubstituted C₂₋₆ alkenyl, substituted or unsubstituted C₂₋₆         alkynyl, substituted or unsubstituted cycloalkyl and substituted         or unsubstituted heterocyclyl;         alternatively, R₅ and R_(5′) taken together with the connecting         C-atom may form an substituted or unsubstituted cycloalkyl or a         substituted or unsubstituted heterocyclyl;         R₆ and R_(6′) are independently selected from hydrogen, halogen,         substituted or unsubstituted C₁₋₆ alkyl, substituted or         unsubstituted C₂₋₆ alkenyl, substituted or unsubstituted C₂₋₆         alkynyl, —CHOR₈ and —C(O)OR₈;     -   wherein R_(a) is selected from hydrogen, substituted or         unsubstituted C₁₋₆ alkyl, substituted or unsubstituted C₂₋₆         alkenyl and substituted or unsubstituted C₂₋₆ alkynyl;         R_(n) is selected from hydrogen, unsubstituted C₁₋₆ alkyl,         unsubstituted C₂₋₆ alkenyl and unsubstituted C₂₋₆ alkynyl;         the alkyl, alkenyl or alkynyl, other than those defined in         R_(1′) or R₂, if substituted, is substituted with one or more         substituent/s selected from —OR₁₃, halogen, —CN, haloalkyl,         haloalkoxy and —NR₁₃R_(13′″);     -   wherein R₁₃ is selected from hydrogen, unsubstituted C₁₋₆ alkyl,         unsubstituted C₂₋₆ alkenyl, and unsubstituted C₂₋₆ alkynyl;     -   R_(13′″) is selected from hydrogen, unsubstituted C₁₋₆ alkyl,         unsubstituted C₂₋₆ alkenyl, unsubstituted C₂₋₆ alkynyl and -Boc;         the aryl, heterocyclyl or cycloalkyl other than those defined in         R_(1′) or R₂, if substituted, is substituted with one or more         substituent/s selected from halogen, —R₁₄, —OR₁₄, —NO₂,         —NR₁₄R_(14′″), NR₁₄C(O)R_(14′), —NR₁₄S(O)₂R_(14′),         —S(O)₂NR₁₄R_(14′), —NR₁₄C(O)NR_(14′)R_(14″), —SR₁₄, —S(O)R₁₄,         S(O)₂R₁₄, —CN, haloalkyl, haloalkoxy, —C(O)OR₁₄,         —C(O)NR₁₄R_(14′), —OCH₂CH₂OH, —NR₁₄S(O)₂NR_(14′)R_(14″) and         C(CH₃)₂OR₁₄;         additionally, wherein cycloalkyl or non-aromatic heterocyclyl,         other than those defined in R_(1′) or R₂, if substituted, may         also be substituted with

or ═O;

-   -   wherein R₁₄, R_(14′) and R_(14″) are independently selected from         hydrogen, unsubstituted C₁₋₆ alkyl, unsubstituted C₂₋₆ alkenyl,         unsubstituted C₂₋₆ alkynyl, unsubstituted aryl, unsubstituted         cycloalkyl and unsubstituted heterocyclyl;     -   and wherein R_(14′″) is selected from hydrogen, unsubstituted         C₁₋₆ alkyl, unsubstituted C₂₋₆ alkenyl, unsubstituted C₂₋₆         alkynyl and -Boc;

These preferred compounds according to the invention are optionally in form of one of the stereoisomers, preferably enantiomers or diastereomers, a racemate or in form of a mixture of at least two of the stereoisomers, preferably enantiomers and/or diastereomers, in any mixing ratio, or a corresponding salt thereof, or a corresponding solvate thereof.

In a further embodiment the compound according to the invention of general Formula (I) is a compound wherein

m is 1, 2, 3, 4 or 5; optionally in form of one of the stereoisomers, preferably enantiomers or diastereomers, a racemate or in form of a mixture of at least two of the stereoisomers, preferably enantiomers and/or diastereomers, in any mixing ratio, or a corresponding salt thereof, or a corresponding solvate thereof.

In a further embodiment the compound according to the invention of general Formula (I) is a compound wherein

n is 0, 1, 2, 3, 4 or 5; optionally in form of one of the stereoisomers, preferably enantiomers or diastereomers, a racemate or in form of a mixture of at least two of the stereoisomers, preferably enantiomers and/or diastereomers, in any mixing ratio, or a corresponding salt thereof, or a corresponding solvate thereof.

In a further embodiment the compound according to the invention of general f Formula (I) is a compound wherein

p is 0, 1 or 2; optionally in form of one of the stereoisomers, preferably enantiomers or diastereomers, a racemate or in form of a mixture of at least two of the stereoisomers, preferably enantiomers and/or diastereomers, in any mixing ratio, or a corresponding salt thereof, or a corresponding solvate thereof.

In a further embodiment the compound according to the invention of general Formula (I) is a compound wherein

X is a bond, —C(R_(x)R_(x′))—, —O—, —C(O)—, —C(O)NR₇—, —NR₇C(O)— or —C(O)O—; optionally in form of one of the stereoisomers, preferably enantiomers or diastereomers, a racemate or in form of a mixture of at least two of the stereoisomers, preferably enantiomers and/or diastereomers, in any mixing ratio, or a corresponding salt thereof, or a corresponding solvate thereof.

In another preferred embodiment of the compound according to the invention of general Formula (I) is a compound wherein

X is a bond; optionally in form of one of the stereoisomers, preferably enantiomers or diastereomers, a racemate or in form of a mixture of at least two of the stereoisomers, preferably enantiomers and/or diastereomers, in any mixing ratio, or a corresponding salt thereof, or a corresponding solvate thereof.

In another preferred embodiment of the compound according to the invention of general Formula (I) is a compound wherein

X is —C(R_(x)R_(x′))—; optionally in form of one of the stereoisomers, preferably enantiomers or diastereomers, a racemate or in form of a mixture of at least two of the stereoisomers, preferably enantiomers and/or diastereomers, in any mixing ratio, or a corresponding salt thereof, or a corresponding solvate thereof.

In another preferred embodiment of the compound according to the invention of general Formula (I) is a compound wherein

X is —O—;

optionally in form of one of the stereoisomers, preferably enantiomers or diastereomers, a racemate or in form of a mixture of at least two of the stereoisomers, preferably enantiomers and/or diastereomers, in any mixing ratio, or a corresponding salt thereof, or a corresponding solvate thereof.

In another preferred embodiment of the compound according to the invention of general Formula (I) is a compound wherein

X is C═O;

optionally in form of one of the stereoisomers, preferably enantiomers or diastereomers, a racemate or in form of a mixture of at least two of the stereoisomers, preferably enantiomers and/or diastereomers, in any mixing ratio, or a corresponding salt thereof, or a corresponding solvate thereof.

In another preferred embodiment of the compound according to the invention of general Formula (I) is a compound wherein

X is —C(O)NR₇—;

optionally in form of one of the stereoisomers, preferably enantiomers or diastereomers, a racemate or in form of a mixture of at least two of the stereoisomers, preferably enantiomers and/or diastereomers, in any mixing ratio, or a corresponding salt thereof, or a corresponding solvate thereof.

In another preferred embodiment of the compound according to the invention of general Formula (I) is a compound wherein

X is —NR₇C(O)—;

optionally in form of one of the stereoisomers, preferably enantiomers or diastereomers, a racemate or in form of a mixture of at least two of the stereoisomers, preferably enantiomers and/or diastereomers, in any mixing ratio, or a corresponding salt thereof, or a corresponding solvate thereof.

In another preferred embodiment of the compound according to the invention of general Formula (I) is a compound wherein

X is —C(O)O—;

optionally in form of one of the stereoisomers, preferably enantiomers or diastereomers, a racemate or in form of a mixture of at least two of the stereoisomers, preferably enantiomers and/or diastereomers, in any mixing ratio, or a corresponding salt thereof, or a corresponding solvate thereof.

In a further embodiment the compound according to the invention of general Formula (I) is a compound wherein

Y is —CH₂— or —C(O)—;

optionally in form of one of the stereoisomers, preferably enantiomers or diastereomers, a racemate or in form of a mixture of at least two of the stereoisomers, preferably enantiomers and/or diastereomers, in any mixing ratio, or a corresponding salt thereof, or a corresponding solvate thereof.

In a further embodiment the compound according to the invention of general Formula (I) is a compound wherein

Y is —CH₂—;

optionally in form of one of the stereoisomers, preferably enantiomers or diastereomers, a racemate or in form of a mixture of at least two of the stereoisomers, preferably enantiomers and/or diastereomers, in any mixing ratio, or a corresponding salt thereof, or a corresponding solvate thereof.

In a further embodiment the compound according to the invention of general Formula (I) is a compound wherein

Y is-C(O)—; optionally in form of one of the stereoisomers, preferably enantiomers or diastereomers, a racemate or in form of a mixture of at least two of the stereoisomers, preferably enantiomers and/or diastereomers, in any mixing ratio, or a corresponding salt thereof, or a corresponding solvate thereof.

In another preferred embodiment of the compound according to the invention of general Formula (I) is a compound wherein

R₁ is

optionally in form of one of the stereoisomers, preferably enantiomers or diastereomers, a racemate or in form of a mixture of at least two of the stereoisomers, preferably enantiomers and/or diastereomers, in any mixing ratio, or a corresponding salt thereof, or a corresponding solvate thereof.

In a further embodiment the compound according to the invention of general Formula (I) is a compound wherein

R_(1′) is selected from substituted or unsubstituted C₁₋₆ alkyl, substituted or unsubstituted C₂₋₆ alkenyl, substituted or unsubstituted C₂₋₆ alkynyl, substituted or unsubstituted cycloalkyl, substituted or unsubstituted aryl and substituted or unsubstituted heterocyclyl; optionally in form of one of the stereoisomers, preferably enantiomers or diastereomers, a racemate or in form of a mixture of at least two of the stereoisomers, preferably enantiomers and/or diastereomers, in any mixing ratio, or a corresponding salt thereof, or a corresponding solvate thereof.

In a further embodiment the compound according to the invention of general Formula (I) is a compound wherein

R_(1′) is selected from substituted or unsubstituted C₁₋₆ alkyl, substituted or unsubstituted C₂₋₆ alkenyl, substituted or unsubstituted C₂₋₆ alkynyl and substituted or unsubstituted aryl; optionally in form of one of the stereoisomers, preferably enantiomers or diastereomers, a racemate or in form of a mixture of at least two of the stereoisomers, preferably enantiomers and/or diastereomers, in any mixing ratio, or a corresponding salt thereof, or a corresponding solvate thereof.

In a further embodiment the compound according to the invention of general Formula (I) is a compound wherein

R_(1′) is selected from substituted or unsubstituted C₁₋₆ alkyl and substituted or unsubstituted aryl; optionally in form of one of the stereoisomers, preferably enantiomers or diastereomers, a racemate or in form of a mixture of at least two of the stereoisomers, preferably enantiomers and/or diastereomers, in any mixing ratio, or a corresponding salt thereof, or a corresponding solvate thereof.

In a further embodiment the compound according to the invention of general Formula (I) is a compound wherein

R₂ is selected from hydrogen, substituted or unsubstituted C₁₋₆ alkyl substituted or unsubstituted C₂₋₆ alkenyl, substituted or unsubstituted C₂₋₆ alkynyl, substituted or unsubstituted cycloalkyl, substituted or unsubstituted aryl and substituted or unsubstituted heterocyclyl; optionally in form of one of the stereoisomers, preferably enantiomers or diastereomers, a racemate or in form of a mixture of at least two of the stereoisomers, preferably enantiomers and/or diastereomers, in any mixing ratio, or a corresponding salt thereof, or a corresponding solvate thereof.

In a further embodiment the compound according to the invention, of general Formula (I) is a compound wherein

R₂ is selected from hydrogen, substituted or unsubstituted C₁₋₆ alkyl, substituted or unsubstituted C₂₋₆ alkenyl, substituted or unsubstituted C₂₋₆ alkynyl and substituted or unsubstituted aryl; optionally in form of one of the stereoisomers, preferably enantiomers or diastereomers, a racemate or in form of a mixture of at least two of the stereoisomers, preferably enantiomers and/or diastereomers, in any mixing ratio, or a corresponding salt thereof, or a corresponding solvate thereof.

In a further embodiment the compound according to the invention of general Formula (I) is a compound wherein:

R₂ is selected from hydrogen, substituted or unsubstituted C₁₋₆ alkyl, and substituted or unsubstituted aryl; optionally in form of one of the stereoisomers, preferably enantiomers or diastereomers, a racemate or in form of a mixture of at least two of the stereoisomers, preferably enantiomers and/or diastereomers, in any mixing ratio, or a corresponding salt thereof, or a corresponding solvate thereof.

In another preferred embodiment of the compound according to the according to the invention of general Formula (I) is a compound wherein

R₃ and R_(3′) are independently selected from hydrogen, substituted or unsubstituted C₁₋₆ alkyl, substituted or unsubstituted C₂₋₆ alkenyl, substituted or unsubstituted C₂₋₆ alkynyl, substituted or unsubstituted cycloalkyl, substituted or unsubstituted alkylcycloalkyl, substituted or unsubstituted alkylaryl, substituted or unsubstituted aryl, substituted or unsubstituted heterocyclyl or substituted or unsubstituted alkylheterocyclyl; optionally in form of one of the stereoisomers, preferably enantiomers or diastereomers, a racemate or in form of a mixture of at least two of the stereoisomers, preferably enantiomers and/or diastereomers, in any mixing ratio, or a corresponding salt thereof, or a corresponding solvate thereof.

In another preferred embodiment of the compound according to the according to the invention of general Formula (I) is a compound wherein

R₃ and R_(3′) are independently selected from hydrogen, substituted or unsubstituted C₁₋₆ alkyl, substituted or unsubstituted C₂₋₆ alkenyl, substituted or unsubstituted C₂₋₆ alkynyl, substituted or unsubstituted cycloalkyl substituted or unsubstituted alkylcycloalkyl, substituted or unsubstituted alkylaryl, substituted or unsubstituted aryl, substituted or unsubstituted heterocyclyl or substituted or unsubstituted alkylheterocyclyl; optionally in form of one of the stereoisomers, preferably enantiomers or diastereomers, a racemate or in form of a mixture of at least two of the stereoisomers, preferably enantiomers and/or diastereomers, in any mixing ratio, or a corresponding salt thereof, or a corresponding solvate thereof.

In another preferred embodiment of the compound according to the according to the invention of general Formula (I) is a compound wherein

R₃ and R_(3′) are independently selected from hydrogen, substituted or unsubstituted C₁₋₆ alkyl, substituted or unsubstituted C₂₋₆ alkenyl and substituted or unsubstituted C₂₋₆ alkynyl; optionally in form of one of the stereoisomers, preferably enantiomers or diastereomers, a racemate or in form of a mixture of at least two of the stereoisomers, preferably enantiomers and/or diastereomers, in any mixing ratio, or a corresponding salt thereof, or a corresponding solvate thereof.

In another preferred embodiment of the compound according to the according to the invention of general Formula (I) is a compound wherein

R₃ and R_(3′) are independently selected from hydrogen and substituted or unsubstituted C₁₋₆ alkyl; optionally in form of one of the stereoisomers, preferably enantiomers or diastereomers, a racemate or in form of a mixture of at least two of the stereoisomers, preferably enantiomers and/or diastereomers, in any mixing ratio, or a corresponding salt thereof, or a corresponding solvate thereof.

In another preferred embodiment of the compound according to the according to the invention of general Formula (I) is a compound wherein

R₃ and R_(3′) taken together with the connecting C-atom may form an substituted or unsubstituted cycloalkyl; optionally in form of one of the stereoisomers, preferably enantiomers or diastereomers, a racemate or in form of a mixture of at least two of the stereoisomers, preferably enantiomers and/or diastereomers, in any mixing ratio, or a corresponding salt thereof, or a corresponding solvate thereof.

In another preferred embodiment of the compound according to the invention of general Formula (I) is a compound wherein

R₄ and R_(4′) are independently selected from hydrogen, substituted or unsubstituted C₁₋₆ alkyl, substituted or unsubstituted C₂₋₆ alkenyl and substituted or unsubstituted C₂₋₆ alkynyl; optionally in form of one of the stereoisomers, preferably enantiomers or diastereomers, a racemate or in form of a mixture of at least two of the stereoisomers, preferably enantiomers and/or diastereomers, in any mixing ratio, or a corresponding salt thereof, or a corresponding solvate thereof.

In another preferred embodiment of the compound according to the invention of general Formula (I) is a compound wherein

R₅ and R_(5′) are independently selected from hydrogen, substituted or unsubstituted C₁₋₆ alkyl, substituted or unsubstituted C₂₋₆ alkenyl and substituted or unsubstituted C₂₋₆ alkynyl; optionally in form of one of the stereoisomers, preferably enantiomers or diastereomers, a racemate or in form of a mixture of at least two of the stereoisomers, preferably enantiomers and/or diastereomers, in any mixing ratio, or a corresponding salt thereof, or a corresponding solvate thereof.

In another preferred embodiment of the compound according to the invention of general Formula (I) is a compound wherein

R₅ and R_(5′) are independently selected from hydrogen and substituted or unsubstituted C₁₋₆ alkyl; optionally in form of one of the stereoisomers, preferably enantiomers or diastereomers, a racemate or in form of a mixture of at least two of the stereoisomers, preferably enantiomers and/or diastereomers, in any mixing ratio, or a corresponding salt thereof, or a corresponding solvate thereof.

In another preferred embodiment of the compound according to the invention of general Formula (I) is a compound wherein

R₅ and R_(5′) taken together with the connecting C-atom may form an substituted or unsubstituted cycloalkyl or a substituted or unsubstituted heterocyclyl; optionally in form of one of the stereoisomers, preferably enantiomers or diastereomers, a racemate or in form of a mixture of at least two of the stereoisomers, preferably enantiomers and/or diastereomers, in any mixing ratio, or a corresponding salt thereof, or a corresponding solvate thereof.

In another preferred embodiment of the compound according to the invention of general Formula (I) is a compound wherein:

R₅ and R_(5′) taken together with the connecting C-atom may form an substituted or unsubstituted cycloalkyl or a substituted or unsubstituted heterocyclyl, m is 1, X is a bond, n is 0 and R₂ is hydrogen; optionally in form of one of the stereoisomers, preferably enantiomers or diastereomers, a racemate or in form of a mixture of at least two of the stereoisomers, preferably enantiomers and/or diastereomers, in any mixing ratio, or a corresponding salt thereof, or a corresponding solvate thereof.

In another preferred embodiment of the compound according to the invention of general Formula (I) is a compound wherein

R₅ and R_(5′) taken together with the connecting C-atom may form an substituted or unsubstituted cycloalkyl or a substituted or unsubstituted non-aromatic heterocyclyl; optionally in form of one of the stereoisomers, preferably enantiomers or diastereomers, a racemate or in form of a mixture of at least two of the stereoisomers, preferably enantiomers and/or diastereomers, in any mixing ratio, or a corresponding salt thereof, or a corresponding solvate thereof.

In another preferred embodiment of the compound according to the invention of general Formula (I) is a compound wherein

R₅ and R_(5′) taken together with the connecting C-atom may form an substituted or unsubstituted cycloalkyl or a substituted or unsubstituted non-aromatic heterocyclyl, m is 1, X is a bond, n is 0 and R₂ is hydrogen; optionally in form of one of the stereoisomers, preferably enantiomers or diastereomers, a racemate or in form of a mixture of at least two of the stereoisomers, preferably enantiomers and/or diastereomers, in any mixing ratio, or a corresponding salt thereof, or a corresponding solvate thereof.

In another preferred embodiment of the compound according to the invention of general Formula (I) is a compound wherein

R₆ and R_(6′) are independently selected from hydrogen, halogen, substituted or unsubstituted C₁₋₆ alkyl, substituted or unsubstituted C₂₋₆ alkenyl, substituted or unsubstituted C₂₋₆ alkynyl, —CHOR₆ and —C(O)OR₈; optionally in form of one of the stereoisomers, preferably enantiomers or diastereomers, a racemate or in form of a mixture of at least two of the stereoisomers, preferably enantiomers and/or diastereomers, in any mixing ratio, or a corresponding salt thereof, or a corresponding solvate thereof.

In another preferred embodiment of the compound according to the invention of general Formula (I) is a compound wherein

R₆ and R_(6′) are independently selected from hydrogen, substituted or unsubstituted C₁₋₆ alkyl, substituted or unsubstituted C₂₋₆ alkenyl and substituted or unsubstituted C₂₋₆ alkynyl; optionally in form of one of the stereoisomers, preferably enantiomers or diastereomers, a racemate or in form of a mixture of at least two of the stereoisomers, preferably enantiomers and/or diastereomers, in any mixing ratio, or a corresponding salt thereof, or a corresponding solvate thereof.

In another preferred embodiment of the compound according to the invention of general Formula (I) is a compound wherein

R₆ and R_(6′) are independently selected from hydrogen and substituted or unsubstituted C₁₋₆ alkyl; optionally in form of one of the stereoisomers, preferably enantiomers or diastereomers, a racemate or in form of a mixture of at least two of the stereoisomers, preferably enantiomers and/or diastereomers, in any mixing ratio, or a corresponding salt thereof, or a corresponding solvate thereof.

In another preferred embodiment of the compound according to the invention of general Formula (I) is a compound wherein

R₇ is selected from hydrogen, substituted or unsubstituted C₁₋₆ alkyl, substituted or unsubstituted C₂₋₆ alkenyl and substituted or unsubstituted C₂₋₆ alkynyl; optionally in form of one of the stereoisomers, preferably enantiomers or diastereomers, a racemate or in form of a mixture of at least two of the stereoisomers, preferably enantiomers and/or diastereomers, in any mixing ratio, or a corresponding salt thereof, or a corresponding solvate thereof.

In another preferred embodiment of the compound according to the invention of general Formula (I) is a compound wherein

R₈ is selected from hydrogen, substituted or unsubstituted C₁₋₆ alkyl, substituted or unsubstituted C₂₋₆ alkenyl and substituted or unsubstituted C₂₋₆ alkynyl; optionally in form of one of the stereoisomers, preferably enantiomers or diastereomers, a racemate or in form of a mixture of at least two of the stereoisomers, preferably enantiomers and/or diastereomers, in any mixing ratio, or a corresponding salt thereof, or a corresponding solvate thereof.

In another preferred embodiment of the compound according to the invention of general Formula (i) is a compound wherein

R₁₁, R_(11′) and R_(11″) are independently selected from hydrogen, unsubstituted C₁₋₆ alkyl, unsubstituted C₂₋₆ alkenyl and unsubstituted C₂₋₆ alkynyl; and wherein R_(11′″) is selected from hydrogen, unsubstituted C₁₋₆ alkyl, unsubstituted C₂₋₆ alkenyl, unsubstituted C₂₋₆ alkynyl and -Boc; optionally in form of one of the stereoisomers, preferably enantiomers or diastereomers, a racemate or in form of a mixture of at least two of the stereoisomers, preferably enantiomers and/or diastereomers, in any mixing ratio, or a corresponding salt thereof, or a corresponding solvate thereof.

In another preferred embodiment of the compound according to the invention of general Formula (I) is a compound wherein

R₁₁, R_(11′) and R_(11″) are independently selected from hydrogen, unsubstituted C₁₋₆ alkyl, unsubstituted C₂₋₆ alkenyl and unsubstituted C₂₋₆ alkynyl; optionally in form of one of the stereoisomers, preferably enantiomers or diastereomers, a racemate or in form of a mixture of at least two of the stereoisomers, preferably enantiomers and/or diastereomers, in any mixing ratio, or a corresponding salt thereof, or a corresponding solvate thereof.

In another preferred embodiment of the compound according to the invention of general Formula (I) is a compound wherein

R_(11′″) is selected from hydrogen, unsubstituted C₁₋₆ alkyl, unsubstituted C₂₋₆ alkenyl, unsubstituted C₂₋₆ alkynyl and -Boc; optionally in form of one of the stereoisomers, preferably enantiomers or diastereomers, a racemate or in form of a mixture of at least two of the stereoisomers, preferably enantiomers and/or diastereomers, in any mixing ratio, or a corresponding salt thereof, or a corresponding solvate thereof.

In another preferred embodiment of the compound according to the invention of general Formula (I) is a compound wherein

R₁₂, R_(12′) and R_(12″) are independently selected from hydrogen, unsubstituted C₁₋₆ alkyl, unsubstituted C₂₋₆ alkenyl and unsubstituted C₂₋₆ alkynyl; and wherein R_(12′″) is selected from hydrogen, unsubstituted C₁₋₆ alkyl, unsubstituted C₂₋₆ alkenyl, unsubstituted C₂₋₆ alkynyl and -Boc; optionally in form of one of the stereoisomers, preferably enantiomers or diastereomers, a racemate or in form of a mixture of at least two of the stereoisomers, preferably enantiomers and/or diastereomers, in any mixing ratio, or a corresponding salt thereof, or a corresponding solvate thereof.

In another preferred embodiment of the compound according to the invention of general Formula (I) is a compound wherein

R₁₂, R_(12′) and R_(12″) are independently selected from hydrogen, unsubstituted C₁₋₆ alkyl, unsubstituted C₂₋₆ alkenyl and unsubstituted C₂₋₆ alkynyl; optionally in form of one of the stereoisomers, preferably enantiomers or diastereomers, a racemate or in form of a mixture of at least two of the stereoisomers, preferably enantiomers and/or diastereomers, in any mixing ratio, or a corresponding salt thereof, or a corresponding solvate thereof.

In another preferred embodiment of the compound according to the invention of general Formula (I) is a compound wherein

R_(12′″) is selected from hydrogen, unsubstituted C₁₋₆ alkyl, unsubstituted C₂₋₆ alkenyl, unsubstituted C₂₋₆, alkynyl and -Boc; optionally in form of one of the stereoisomers, preferably enantiomers or diastereomers, a racemate or in form of a mixture of at least two of the stereoisomers, preferably enantiomers and/or diastereomers, in any mixing ratio, or a corresponding salt thereof, or a corresponding solvate thereof.

In another preferred embodiment of the compound according to the invention of general Formula (I) is a compound wherein.

R₁₃ is selected from hydrogen, unsubstituted C₁₋₆ alkyl, unsubstituted C₂₋₆alkenyl, and unsubstituted C₂₋₆ alkynyl; R_(13′″) is selected from hydrogen, unsubstituted C₁₋₆ alkyl, unsubstituted C₂₋₆ alkenyl, unsubstituted C₂₋₆ alkynyl and -Boc; optionally in form of one of the stereoisomers, preferably enantiomers or diastereomers, a racemate or in form of a mixture of at least two of the stereoisomers, preferably enantiomers and/or diastereomers, in any mixing ratio, or a corresponding salt thereof, or a corresponding solvate thereof.

In another preferred embodiment of the compound according to the invention of general Formula (I) is a compound wherein

R₁₃ is selected from hydrogen, unsubstituted C₁₋₆ alkyl, unsubstituted C₂₋₆ alkenyl, and unsubstituted C₂₋₆ alkynyl; optionally in form of one of the stereoisomers, preferably enantiomers or diastereomers, a racemate or in form of a mixture of at least two of the stereoisomers, preferably enantiomers and/or diastereomers, in any mixing ratio, or a corresponding salt thereof, or a corresponding solvate thereof.

In another preferred embodiment of the compound according to the invention of general Formula (I) is a compound wherein

R_(13′″) is selected from hydrogen, unsubstituted C₁₋₆ alkyl, unsubstituted C₂₋₆ alkenyl, unsubstituted C₂₋₆ alkynyl and -Boc; optionally in form of one of the stereoisomers, preferably enantiomers or diastereomers, a racemate or in form of a mixture of at least two of the stereoisomers, preferably enantiomers and/or diastereomers, in any mixing ratio, or a corresponding salt thereof, or a corresponding solvate thereof.

In another preferred embodiment of the compound according to the invention of general Formula (I) is a compound wherein

R₁₄, R_(14′) and R_(14″) are independently selected from hydrogen, unsubstituted C₁₋₆ alkyl, unsubstituted C₂₋₆ alkenyl, unsubstituted C₂₋₆ alkynyl, unsubstituted aryl, unsubstituted cycloalkyl and unsubstituted heterocyclyl; and wherein R_(14′″) is selected from hydrogen, unsubstituted C₁₋₆ alkyl, unsubstituted C₂₋₆ alkenyl, unsubstituted C₂₋₆ alkynyl and -Boc; optionally in form of one of the stereoisomers, preferably enantiomers or diastereomers, a racemate or in form of a mixture of at least two of the stereoisomers, preferably enantiomers and/or diastereomers, in any mixing ratio, or a corresponding salt thereof, or a corresponding solvate thereof.

In another preferred embodiment of the compound according to the invention of general Formula (I) is a compound wherein

R₁₄, R_(14′) and R_(14″) are independently selected from hydrogen, unsubstituted C₁₋₆ alkyl, unsubstituted C₂₋₆ alkenyl, unsubstituted C₂₋₆ alkynyl, unsubstituted aryl, unsubstituted cycloalkyl and unsubstituted heterocyclyl; optionally in form of one of the stereoisomers, preferably enantiomers or diastereomers, a racemate or in form of a mixture of at least two of the stereoisomers, preferably enantiomers and/or diastereomers, in any mixing ratio, or a corresponding salt thereof, or a corresponding solvate thereof.

In another preferred embodiment of the compound according to the invention of general Formula (I) is a compound wherein

R_(14′″) is selected from hydrogen, unsubstituted C₁₋₆ alkyl, unsubstituted C₂₋₆ alkenyl, unsubstituted C₂₋₆ alkynyl and -Boc; optionally in form of one of the stereoisomers, preferably enantiomers or diastereomers, a racemate or in form of a mixture of at least two of the stereoisomers, preferably enantiomers and/or diastereomers, in any mixing ratio, or a corresponding salt thereof, or a corresponding solvate thereof.

In another preferred embodiment of the compound according to the invention of general Formula (I) is a compound wherein:

R_(x) is selected from halogen, —OR₇, substituted or unsubstituted C₁₋₆ alkyl, substituted or unsubstituted C₂₋₆ alkenyl and substituted or unsubstituted C₂₋₆ alkynyl; R_(x′) is selected from hydrogen, halogen, substituted or unsubstituted C₁₋₆ alkyl, substituted or unsubstituted C₂₋₆ alkenyl and substituted or unsubstituted C₂₋₆ alkynyl; optionally in form of one of the stereoisomers, preferably enantiomers or diastereomers, a racemate or in form of a mixture of at least two of the stereoisomers, preferably enantiomers and/or diastereomers, in any mixing ratio, or a corresponding salt thereof, or a corresponding solvate thereof.

In another preferred embodiment of the compound according to the invention of general Formula (I) is a compound wherein

R_(x) is selected from halogen, —OR₇, substituted or unsubstituted C₁₋₆ alkyl, substituted or unsubstituted C₂₋₆ alkenyl and substituted or unsubstituted C₂₋₆ alkynyl; optionally in form of one of the stereoisomers, preferably enantiomers or diastereomers, a racemate or in form of a mixture of at least two of the stereoisomers, preferably enantiomers and/or diastereomers, in any mixing ratio, or a corresponding salt thereof, or a corresponding solvate thereof.

In another preferred embodiment of the compound according to the invention of general Formula (I) is a compound wherein

R_(x′) is selected from hydrogen, halogen, substituted or unsubstituted C₁₋₆ alkyl, substituted or unsubstituted C₂₋₆ alkenyl and substituted or unsubstituted C₂₋₆ alkynyl; optionally in form of one of the stereoisomers, preferably enantiomers or diastereomers, a racemate or in form of a mixture of at least two of the stereoisomers, preferably enantiomers and/or diastereomers, in any mixing ratio, or a corresponding salt thereof, or a corresponding solvate thereof.

In another preferred embodiment of the compound according to the invention of general Formula (I) is a compound wherein

R_(n) is selected from hydrogen, unsubstituted C₁₋₆ alkyl, unsubstituted C₂₋₆ alkenyl and unsubstituted C₂₋₆ alkynyl; optionally in form of one of the stereoisomers, preferably enantiomers or diastereomers, a racemate or in form of a mixture of at least two of the stereoisomers, preferably enantiomers and/or diastereomers, in any mixing ratio, or a corresponding salt thereof, or a corresponding solvate thereof.

In another preferred embodiment of the compound according to the invention of general Formula (I) is a compound wherein

R_(n) is selected from hydrogen and unsubstituted C₁₋₆ alkyl; optionally in form of one of the stereoisomers, preferably enantiomers or diastereomers, a racemate or in form of a mixture of at least two of the stereoisomers, preferably enantiomers and/or diastereomers, in any mixing ratio, or a corresponding salt thereof, or a corresponding solvate thereof.

In another preferred embodiment of the compound according to the invention of general Formula (I), is a compound wherein

R₁ is

m is 1, 2, 3, 4 or 5; n is 0, 1, 2, 3, 4 or 5; p is 0, 1 or 2;

Y is —CH₂— or —C(O)—;

X is a bond, —C(R_(x)R_(x′))—, —O—, —C(O)—, —C(O)NR₇—, —NR₇C(O)— or —C(O)O—; R_(1′) is selected from: substituted or unsubstituted C₁₋₆ alkyl, substituted or unsubstituted C₂₋₆ alkenyl, substituted or unsubstituted C₂₋₆ alkynyl, substituted or unsubstituted cycloalkyl, substituted or unsubstituted aryl and substituted or unsubstituted heterocyclyl; wherein the C₁₋₆ alkyl is preferably selected from methyl, ethyl, propyl, butyl, pentyl, hexyl, isopropyl and 2-methylpropyl; more preferably the C₁₋₆ alkyl is methyl or ethyl; and/or the C₂₋₆-alkenyl is preferably selected from ethylene, propylene, butylene, pentylene and hexylene; and/or the C₂₋₆-alkynyl is preferably selected from ethyne, propyne, butyne, pentyne and hexyne; and/or the aryl is selected from phenyl, naphtyl, or anthracene; preferably is napthyl or phenyl; more preferably is phenyl; and/or the heterocyclyl is a heterocyclic ring system of one or more saturated or unsaturated rings of which at least one ring contains one or more heteroatoms from the group consisting of nitrogen, oxygen and/or sulfur in the ring; preferably is a heterocyclic ring system of one or two saturated or unsaturated rings of which at least one ring contains one or more heteroatoms from the group consisting of nitrogen, oxygen and/or sulfur in the ring, more preferably is selected from imidazole, oxadiazole, tetrazole, pyridine, pyrimidine, piperidine, piperazine, benzofuran, benzimidazole, indazole, benzothiazole, benzodiazole, thiazole, benzothiazole, tetrahydropyrane, morpholine, indoline, furan, triazole, isoxazole, pyrazole, thiophene, benzothiophene, pyrrole, pyrazine, pyrrolo[2,3b]pyridine, quinoline, isoquinoline, phthalazine, benzo-1,2,5-thiadiazole, indole, benzotriazole, benzoxazole oxopyrrolidine, pyrimidine, benzodioxolane, benzodioxane, carbazole and quinazoline; and/or the cycloalkyl is C₃₋₈ cycloalkyl like cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, cycloheptyl, or cyclooctyl; preferably is C₃₋₇ cycloalkyl like cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, or cycloheptyl; more preferably from C₃₋₆ cycloalkyl like cyclopropyl, cyclobutyl, cyclopentyl or cyclohexyl;

-   -   and/or         R₂ is selected from hydrogen, substituted or unsubstituted C₁₋₆         alkyl, substituted or unsubstituted C₂₋₆ alkenyl, substituted or         unsubstituted C₂₋₆ alkynyl, substituted or unsubstituted         cycloalkyl, substituted or unsubstituted aryl and substituted or         unsubstituted heterocyclyl;         wherein         the C₁₋₆ alkyl is preferably selected from methyl, ethyl,         propyl, butyl, pentyl, hexyl, isopropyl and 2-methylpropyl; more         preferably the C₁₋₆ alkyl is isopropyl or isobutyl;         and/or         the C₂₋₆-alkenyl is preferably selected from ethylene,         propylene, butylene, pentylene and hexylene;         and/or         the C₂₋₆-alkynyl is preferably selected from ethyne, propyne,         butyne, pentyne and hexyne;         and/or         the aryl is selected from phenyl, naphtyl, or anthracene;         preferably is napthyl or phenyl; more preferably is phenyl;         and/or         the heterocyclyl is a heterocyclic ring system of one or more         saturated or unsaturated rings of which at least one ring         contains one or more heteroatoms from the group consisting of         nitrogen, oxygen and/or sulfur in the ring; preferably is a         heterocyclic ring system of one or two saturated or unsaturated         rings of which at least one ring contains one or more         heteroatoms from the group consisting of nitrogen, oxygen and/or         sulfur in the ring, more preferably is selected from imidazole,         oxadiazole, tetrazole, pyridine, pyrimidine, piperidine,         piperazine, benzofuran, benzimidazole, indazole, benzothiazole,         benzodiazole, thiazole, benzothiazole, tetrahydropyrane,         morpholine, indoline, furan, triazole, isoxazole, pyrazole,         thiophene, benzothiophene, pyrrole, pyrazine,         pyrrolo[2,3b]pyridine, quinoline, isoquinoline, phthalazine,         benzo-1,2,5-thiadiazole, indole, benzotriazole, benzoxazole         oxopyrrolidine, pyrimidine, benzodioxolane, benzodioxane,         carbazole and quinazoline;         and/or         the cycloalkyl is C₃₋₈ cycloalkyl like cyclopropyl, cyclobutyl,         cyclopentyl, cyclohexyl, cycloheptyl, or cyclooctyl; preferably         is C₃₋₇ cycloalkyl like cyclopropyl, cyclobutyl, cyclopentyl,         cyclohexyl, or cycloheptyl; more preferably from C₃₋₆ cycloalkyl         like cyclopropyl, cyclobutyl, cyclopentyl or cyclohexyl;     -   and/or         R₃ and R_(3′) are independently selected from hydrogen,         substituted or unsubstituted C₁₋₆ alkyl, substituted or         unsubstituted C₂₋₆ alkenyl, substituted or unsubstituted C₂₋₆         alkynyl, substituted or unsubstituted cycloalkyl, substituted or         unsubstituted alkylcycloalkyl, substituted or unsubstituted         alkylaryl, substituted or unsubstituted aryl, substituted or         unsubstituted heterocyclyl or substituted or unsubstituted         alkylheterocyclyl;     -   wherein         the C₁₋₆ alkyl is preferably selected from methyl, ethyl,         propyl, butyl, pentyl, hexyl, isopropyl and 2-methylpropyl;         preferably the C₁₋₆ alkyl is methyl;         and/or         the C₂₋₆-alkenyl is preferably selected from ethylene,         propylene, butylene, pentylene and hexylene;         and/or         the C₂₋₆-alkynyl is preferably selected from ethyne, propyne,         butyne, pentyne and hexyne;         and/or         the aryl is selected from phenyl, naphtyl, or anthracene;         preferably is napthyl or phenyl;         and/or         the heterocyclyl is a heterocyclic ring system of one or more         saturated or unsaturated rings of which at least one ring         contains one or more heteroatoms from the group consisting of         nitrogen, oxygen and/or sulfur in the ring; preferably is a         heterocyclic ring system of one or two saturated or unsaturated         rings of which at least one ring contains one or more         heteroatoms from the group consisting of nitrogen, oxygen and/or         sulfur in the ring, more preferably is selected from imidazole,         oxadiazole, tetrazole, pyridine, pyrimidine, piperidine,         piperazine, benzofuran, benzimidazole, indazole, benzothiazole,         benzodiazole, thiazole, benzothiazole, tetrahydropyrane,         morpholine, indoline, furan, triazole, isoxazole, pyrazole,         thiophene, benzothiophene, pyrrole, pyrazine,         pyrrolo[2,3b]pyridine, quinoline, isoquinoline, phthalazine,         benzo-1,2,5-thiadiazole, indole, benzotriazole, benzoxazole         oxopyrrolidine, pyrimidine, benzodioxolane, benzodioxane,         carbazole and quinazoline;         and/or         the cycloalkyl is C₃₋₈ cycloalkyl like cyclopropyl, cyclobutyl,         cyclopentyl, cyclohexyl; cycloheptyl, or cyclooctyl; preferably         is C₃₋₇ cycloalkyl like cyclopropyl, cyclobutyl, cyclopentyl,         cyclohexyl, or cycloheptyl; more preferably from C₃₋₆ cycloalkyl         like cyclopropyl, cyclobutyl, cyclopentyl or cyclohexyl;         and/or         R₃ and R_(3′) taken together with the connecting C-atom may form         an substituted or unsubstituted cycloalkyl;     -   wherein         the cycloalkyl is C₃₋₈ cycloalkyl like cyclopropyl, cyclobutyl,         cyclopentyl, cyclohexyl, cycloheptyl, or cyclooctyl; preferably         is C₃₋₇ cycloalkyl like cyclopropyl, cyclobutyl, cyclopentyl,         cyclohexyl, or cycloheptyl; more preferably from C₃₋₆ cycloalkyl         like cyclopropyl, cyclobutyl, cyclopentyl or cyclohexyl; more         preferably the cycloalkyl is cyclopropyl;         and/or         R₄ and R_(4′) are independently selected from hydrogen,         substituted or unsubstituted C₁₋₆ alkyl, substituted or         unsubstituted C₂₋₆ alkenyl and substituted or unsubstituted C₂₋₆         alkynyl;         wherein         the C₁₋₆ alkyl is preferably selected from methyl, ethyl,         propyl, butyl, pentyl, hexyl, isopropyl and 2-methylpropyl;         and/or         the C₂₋₆-alkenyl is preferably selected from ethylene,         propylene, butylene, pentylene and hexylene;         and/or         the C₂₋₆-alkynyl is preferably selected from ethyne, propyne,         butyne, pentyne and hexyne;         and/or         R₅ and R_(5′) are independently selected from hydrogen,         substituted or unsubstituted C₁₋₆ alkyl, substituted or         unsubstituted C₂₋₆ alkenyl and substituted or unsubstituted C₂₋₆         alkynyl;         alternatively, R₅ and R_(5′) taken together with the connecting         C-atom may form an substituted or unsubstituted cycloalkyl or a         substituted or unsubstituted heterocyclyl;         wherein         the C₁₋₆ alkyl is preferably selected from methyl, ethyl,         propyl, butyl, pentyl, hexyl, isopropyl and 2-methylpropyl; more         preferably the C₁₋₆alkyl is methyl;         and/or         the C₂₋₆-alkenyl is preferably selected from ethylene,         propylene, butylene, pentylene and hexylene;         and/or         the C₂₋₆-alkynyl is preferably selected from ethyne, propyne,         butyne, pentyne and hexyne;         and/or         the heterocyclyl is a heterocyclic ring system of one or more         saturated or unsaturated rings of which at least one ring         contains one or more heteroatoms from the group consisting of         nitrogen, oxygen and/or sulfur in the ring; preferably is a         heterocyclic ring system of one or two saturated or unsaturated         rings of which at least one ring contains one or more         heteroatoms from the group consisting of nitrogen, oxygen and/or         sulfur in the ring, more preferably is selected from imidazole,         oxadiazole, tetrazole, pyridine, pyrimidine, piperidine,         piperazine, benzofuran, benzimidazole, indazole, benzothiazole,         benzodiazole, thiazole, benzothiazole, tetrahydropyrane,         morpholine, indoline, furan, triazole, isoxazole, pyrazole,         thiophene, benzothiophene, pyrrole, pyrazine,         pyrrolo[2,3b]pyridine, quinoline, isoquinoline, phthalazine,         benzo-1,2,5-thiadiazole, indole, benzotriazole, benzoxazole         oxopyrrolidine, pyrimidine, benzodioxolane, benzodioxane,         carbazole and quinazoline; preferably, the heterocyclyl is         non-aromatic heterocyclyl;         and/or         the cycloalkyl is C₃₋₈ cycloalkyl like cyclopropyl, cyclobutyl,         cyclopentyl, cyclohexyl, cycloheptyl, or cyclooctyl; preferably         is C₃₋₇ cycloalkyl like cyclopropyl, cyclobutyl, cyclopentyl,         cyclohexyl, or cycloheptyl; more preferably from C₃₋₆ cycloalkyl         like cyclopropyl, cyclobutyl, cyclopentyl or cyclohexyl;         and/or         R₆ and R_(6′) are independently selected from hydrogen, halogen,         substituted or unsubstituted C₁₋₆ alkyl, substituted or         unsubstituted C₂₋₆ alkenyl, substituted or unsubstituted C₂₋₆         alkynyl, —CHOR₈ and —C(O)OR₈;         wherein         the C₁₋₆ alkyl is preferably selected from methyl, ethyl,         propyl, butyl, pentyl, hexyl, isopropyl and 2-methylpropyl; more         preferably the C₁₋₆ alkyl is methyl;         and/or         the C₂₋₆-alkenyl is preferably selected from ethylene,         propylene, butylene, pentylene and hexylene;         and/or         the C₂₋₆-alkynyl is preferably selected from ethyne, propyne,         butyne, pentyne and hexyne;         and/or         R₇ is selected from hydrogen, substituted or unsubstituted C₁₋₆         alkyl, substituted or unsubstituted C₂₋₆ alkenyl and substituted         or unsubstituted C₂₋₆ alkynyl;         wherein         the C₁₋₆ alkyl is preferably selected from methyl, ethyl,         propyl, butyl, pentyl, hexyl, isopropyl and 2-methylpropyl;         and/or         the C₂₋₆-alkenyl is preferably selected from ethylene,         propylene, butylene, pentylene and hexylene;         and/or         the C₂₋₆-alkynyl is preferably selected from ethyne, propyne,         butyne, pentyne and hexyne;         and/or         R₈ is selected from hydrogen, substituted or unsubstituted C₁₋₆         alkyl, substituted or unsubstituted C₂₋₆ alkenyl and substituted         or unsubstituted C₂₋₆ alkynyl;         wherein         the C₁₋₆ alkyl is preferably selected from methyl, ethyl,         propyl, butyl, pentyl, hexyl, isopropyl and 2-methylpropyl;         and/or         the C₂₋₆-alkenyl is preferably selected from ethylene,         propylene, butylene, pentylene and hexylene;         and/or         the C₂₋₆-alkynyl is preferably selected from ethyne, propyne,         butyne, pentyne and hexyne;         and/or         R₁₁, R_(11′) and R_(11″) are independently selected from         hydrogen, unsubstituted C₁₋₆ alkyl, unsubstituted C₂₋₆ alkenyl         and unsubstituted C₂₋₆ alkynyl;         and wherein R_(11′″) is selected from hydrogen, unsubstituted         C₁₋₆ alkyl, unsubstituted C₂₋₆ alkenyl, unsubstituted C₂₋₆         alkynyl and -Boc;         wherein         the C₁₋₆ alkyl is preferably selected from methyl, ethyl,         propyl, butyl, pentyl, hexyl, isopropyl and 2-methylpropyl;         and/or         the C₂₋₆-alkenyl is preferably selected from ethylene,         propylene, butylene, pentylene and hexylene;         and/or         the C₂₋₆-alkynyl is preferably selected from ethyne, propyne,         butyne, pentyne and hexyne;         and/or         R₁₂, R_(12′) and R_(12″) are independently selected from         hydrogen, unsubstituted C₁₋₆ alkyl, unsubstituted C₂₋₆ alkenyl         and unsubstituted C₂₋₆ alkynyl;         and wherein R_(12′″) is selected from hydrogen, unsubstituted         C₁₋₆ alkyl, unsubstituted C₂₋₆ alkenyl, unsubstituted C₂₋₆         alkynyl and -Boc;         wherein         the C₁₋₆ alkyl is preferably selected from methyl, ethyl,         propyl, butyl, pentyl, hexyl, isopropyl and 2-methylpropyl;         and/or         the C₂₋₆-alkenyl is preferably selected from ethylene,         propylene, butylene, pentylene and hexylene;         and/or         the C₂₋₆-alkynyl is preferably selected from ethyne, propyne,         butyne, pentyne and hexyne;         and/or         R₁₃ is selected from hydrogen, unsubstituted C₁₋₆ alkyl,         unsubstituted C₂₋₆ alkenyl, and unsubstituted C₂₋₆ alkynyl;         R_(13′″) is selected from hydrogen, unsubstituted C₁₋₆ alkyl,         unsubstituted C₂₋₆ alkenyl, unsubstituted C₂₋₆ alkynyl and -Boc;         wherein         the C₁₋₆ alkyl is preferably selected from methyl, ethyl,         propyl, butyl, pentyl, hexyl, isopropyl and 2-methylpropyl;         and/or         the C₂₋₆-alkenyl is preferably selected from ethylene,         propylene, butylene, pentylene and hexylene;         and/or         the C₂₋₆-alkynyl is preferably selected from ethyne, propyne,         butyne, pentyne and hexyne;         and/or         R₁₄, R_(14′) and R_(14″) are independently selected from         hydrogen, unsubstituted C₁₋₆ alkyl, unsubstituted C₂₋₆ alkenyl,         unsubstituted C₂₋₆ alkynyl, unsubstituted aryl, unsubstituted         cycloalkyl and unsubstituted heterocyclyl;         and wherein R_(14′″) is selected from hydrogen, unsubstituted         C₁₋₆ alkyl, unsubstituted C₂₋₆ alkenyl, unsubstituted C₂₋₆         alkynyl and -Boc;         wherein         the C₁₋₆ alkyl is preferably selected from methyl, ethyl,         propyl, butyl, pentyl, hexyl, isopropyl and 2-methylpropyl;         and/or         the C₂₋₆-alkenyl is preferably selected from ethylene,         propylene, butylene, pentylene and hexylene;         and/or         the C₂₋₆-alkynyl is preferably selected from ethyne, propyne,         butyne, pentyne and hexyne;         and/or         the aryl is selected from phenyl, naphtyl and anthracene;         preferably is napthyl or phenyl;         and/or         the heterocyclyl is a heterocyclic ring system of one or more         saturated or unsaturated rings of which at least one ring         contains one or more heteroatoms from the group consisting of         nitrogen, oxygen and/or sulfur in the ring; preferably is a         heterocyclic ring system of one or two saturated or unsaturated         rings of which at least one ring contains one or more         heteroatoms from the group consisting of nitrogen, oxygen and/or         sulfur in the ring, more preferably is selected from imidazole,         oxadiazole, tetrazole, pyridine, pyrimidine, piperidine,         piperazine, benzofuran, benzimidazole, indazole, benzothiazole,         benzodiazole, thiazole, benzothiazole, tetrahydropyrane,         morpholine, indoline, furan, triazole, isoxazole, pyrazole,         thiophene, benzothiophene, pyrrole, pyrazine,         pyrrolo[2,3b]pyridine, quinoline, isoquinoline, phthalazine,         benzo-1,2,5-thiadiazole, indole, benzotriazole, benzoxazole         oxopyrrolidine, pyrimidine, benzodioxolane, benzodioxane,         carbazole and quinazoline;         and/or         the cycloalkyl is C₃₋₈ cycloalkyl like cyclopropyl, cyclobutyl,         cyclopentyl, cyclohexyl, cycloheptyl, or cyclooctyl; preferably         is C₃₋₇ cycloalkyl like cyclopropyl, cyclobutyl, cyclopentyl,         cyclohexyl, or cycloheptyl; more preferably from C₃₋₆ cycloalkyl         like cyclopropyl, cyclobutyl, cyclopentyl or cyclohexyl;         and/or         R_(x) is selected from halogen, —OR₇, substituted or         unsubstituted C₁₋₆ alkyl, substituted or unsubstituted C₂₋₆         alkenyl and substituted or unsubstituted C₂₋₆ alkynyl;         wherein         the C₁₋₆ alkyl is preferably selected from methyl, ethyl,         propyl, butyl, pentyl, hexyl, isopropyl and 2-methylpropyl;         and/or         the C₂₋₆-alkenyl is preferably selected from ethylene,         propylene, butylene, pentylene and hexylene;         and/or         the C₂₋₆-alkynyl is preferably selected from ethyne, propyne,         butyne, pentyne and hexyne;         and/or         R_(x′) is selected from hydrogen, halogen, substituted or         unsubstituted C₁₋₆ alkyl, substituted or unsubstituted C₂₋₆         alkenyl and substituted or unsubstituted C₂₋₆ alkynyl;         wherein         the C₁₋₆ alkyl is preferably selected from methyl, ethyl,         propyl, butyl, pentyl, hexyl, isopropyl and 2-methylpropyl;         and/or         the C₂₋₆-alkenyl is preferably selected from ethylene,         propylene, butylene, pentylene and hexylene;         and/or         the C₂₋₆-alkynyl is preferably selected from ethyne, propyne,         butyne, pentyne and hexyne;         and/or         R_(n) is selected from hydrogen, unsubstituted C₁₋₆ alkyl,         unsubstituted C₂₋₆ alkenyl and unsubstituted C₂₋₆ alkynyl;         wherein         the C₁₋₆ alkyl is preferably selected from methyl, ethyl,         propyl, butyl, pentyl, hexyl, isopropyl and 2-methylpropyl,         preferably the C₁₋₆ alkyl is methyl;         and/or         the C₂₋₆-alkenyl is preferably selected from ethylene,         propylene, butylene, pentylene and hexylene;         and/or         the C₂₋₆-alkynyl is preferably selected from ethyne, propyne,         butyne, pentyne and hexyne;         optionally in form of one of the stereoisomers, preferably         enantiomers or diastereomers, a racemate or in form of a mixture         of at least two of the stereoisomers, preferably enantiomers         and/or diastereomers, in any mixing ratio, or a corresponding         salt thereof, or a corresponding solvate thereof.

In another preferred embodiment of the invention according to general Formula (I) the compound is a compound, wherein in R_(1′) as defined in any of the embodiments of the present invention,

the C₁₋₆ alkyl is preferably selected from methyl, ethyl, propyl, butyl, pentyl, hexyl, isopropyl and 2-methylpropyl; more preferably the C₁₋₆ alkyl is methyl or ethyl; and/or the C₂₋₆-alkenyl is preferably selected from ethylene, propylene, butylene, pentylene and hexylene; and/or the C₂₋₆-alkynyl is preferably selected from ethyne, propyne, butyne, pentyne and hexyne; and/or the aryl is selected from phenyl, naphtyl, or anthracene; preferably is napthyl or phenyl; more preferably is phenyl; and/or the heterocyclyl is a heterocyclic ring system of one or more saturated or unsaturated rings of which at least one ring contains one or more heteroatoms from the group consisting of nitrogen, oxygen and/or sulfur in the ring; preferably is a heterocyclic ring system of one or two saturated or unsaturated rings of which at least one ring contains one or more heteroatoms from the group consisting of nitrogen, oxygen and/or sulfur in the ring, more preferably is selected from imidazole, oxadiazole, tetrazole, pyridine, pyrimidine, piperidine, piperazine, benzofuran, benzimidazole, indazole, benzothiazole, benzodiazole, thiazole, benzothiazole, tetrahydropyrane, morpholine, indoline, furan, triazole, isoxazole, pyrazole, thiophene, benzothiophene, pyrrole, pyrazine, pyrrolo[2,3b]pyridine, quinoline, isoquinoline, phthalazine, benzo-1,2,5-thiadiazole, indole, benzotriazole, benzoxazole oxopyrrolidine, pyrimidine, benzodioxolane, benzodioxane, carbazole and quinazoline; and/or the cycloalkyl is C₃₋₈ cycloalkyl like cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, cycloheptyl, or cyclooctyl; preferably is C₃₋₇ cycloalkyl like cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, or cycloheptyl; more preferably from C₃₋₆ cycloalkyl like cyclopropyl, cyclobutyl, cyclopentyl or cyclohexyl; optionally in form of one of the stereoisomers, preferably enantiomers or diastereomers, a racemate or in form of a mixture of at least two of the stereoisomers, preferably enantiomers and/or diastereomers, in any mixing ratio, or a corresponding salt thereof, or a corresponding solvate thereof.

In another preferred embodiment of the invention according to general Formula (I) the compound is a compound, wherein: in R₂ as defined in any of the embodiments of the present invention,

the C₁₋₆ alkyl is preferably selected from methyl, ethyl, propyl, butyl, pentyl, hexyl, isopropyl and 2-methylpropyl; more preferably the C₁₋₆ alkyl is isopropyl or isobutyl; and/or the C₂₋₆-alkenyl is preferably selected from ethylene, propylene, butylene, pentylene and hexylene; and/or the C₂₋₆-alkynyl is preferably selected from ethyne, propyne, butyne, pentyne and hexyne; and/or the aryl is selected from phenyl, naphtyl, or anthracene; preferably is napthyl or phenyl; more preferably is phenyl; and/or the heterocyclyl is a heterocyclic ring system of one or more saturated or unsaturated rings of which at least one ring contains one or more heteroatoms from the group consisting of nitrogen, oxygen and/or sulfur in the ring; preferably is a heterocyclic ring system of one or two saturated or unsaturated rings of which at least one ring contains one or more heteroatoms from the group consisting of nitrogen, oxygen and/or sulfur in the ring, more preferably is selected from imidazole, oxadiazole, tetrazole, pyridine, pyrimidine, piperidine, piperazine, benzofuran, benzimidazole, indazole, benzothiazole, benzodiazole, thiazole, benzothiazole, tetrahydropyrane, morpholine, indoline, furan, triazole, isoxazole, pyrazole, thiophene, benzothiophene, pyrrole, pyrazine, pyrrolo[2,3b]pyridine, quinoline, isoquinoline, phthalazine, benzo-1,2,5-thiadiazole, indole, benzotriazole, benzoxazole oxopyrrolidine, pyrimidine, benzodioxolane, benzodioxane, carbazole and quinazoline; and/or the cycloalkyl is C₃₋₈ cycloalkyl like cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, cycloheptyl, or cyclooctyl; preferably is C₃₋₇ cycloalkyl like cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, or cycloheptyl; more preferably from C₃₋₆ cycloalkyl like cyclopropyl, cyclobutyl, cyclopentyl or cyclohexyl; optionally in form of one of the stereoisomers, preferably enantiomers or diastereomers, a racemate or in form of a mixture of at least two of the stereoisomers, preferably enantiomers and/or diastereomers, in any mixing ratio, or a corresponding salt thereof, or a corresponding solvate thereof.

In another preferred embodiment of the invention according to general Formula (I) the compound is a compound, wherein in R₃ and R_(3′) as defined in any of the embodiments of the present invention,

the C₁₋₆ alkyl is preferably selected from methyl, ethyl, propyl, butyl, pentyl, hexyl, isopropyl and 2-methylpropyl; and/or the C₂₋₆-alkenyl is preferably selected from ethylene, propylene, butylene, pentylene and hexylene; and/or the C₂₋₆-alkynyl is preferably selected from ethyne, propyne, butyne, pentyne and hexyne; and/or the aryl is selected from phenyl, naphtyl, or anthracene; preferably is napthyl or phenyl; and/or the heterocyclyl is a heterocyclic ring system of one or more saturated or unsaturated rings of which at least one ring contains one or more heteroatoms from the group consisting of nitrogen, oxygen and/or sulfur in the ring; preferably is a heterocyclic ring system of one or two saturated or unsaturated rings of which at least one ring contains one or more heteroatoms from the group consisting of nitrogen, oxygen and/or sulfur in the ring, more preferably is selected from imidazole, oxadiazole, tetrazole, pyridine, pyrimidine, piperidine, piperazine, benzofuran, benzimidazole, indazole, benzothiazole, benzodiazole, thiazole, benzothiazole, tetrahydropyrane, morpholine, indoline, furan, triazole, isoxazole, pyrazole, thiophene, benzothiophene, pyrrole, pyrazine, pyrrolo[2,3b]pyridine, quinoline, isoquinoline, phthalazine, benzo-1,2,5-thiadiazole, indole, benzotriazole, benzoxazole oxopyrrolidine, pyrimidine, benzodioxolane, benzodioxane, carbazole and quinazoline; and/or the cycloalkyl is C₃₋₈, cycloalkyl like cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, cycloheptyl, or cyclooctyl; preferably is C₃₋₇ cycloalkyl like cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, or cycloheptyl; more preferably from C₃₋₆ cycloalkyl like cyclopropyl, cyclobutyl, cyclopentyl or cyclohexyl; more preferably the cycloalkyl is cyclopropyl; optionally in form of one of the stereoisomers, preferably enantiomers or diastereomers, a racemate or in form of a mixture of at least two of the stereoisomers, preferably enantiomers and/or diastereomers, in any mixing ratio, or a corresponding salt thereof, or a corresponding solvate thereof.

In another preferred embodiment of the invention according to general Formula (I) the compound is a compound, wherein in R₃ and R_(3′) as defined in any of the embodiments of the present invention,

the C₁₋₆ alkyl is preferably selected from methyl, ethyl, propyl, butyl, pentyl, hexyl, isopropyl and 2-methylpropyl; preferably the C₁₋₆ alkyl is methyl; and/or the C₂₋₆-alkenyl is preferably selected from ethylene, propylene, butylene, pentylene and hexylene; and/or the C₂₋₆-alkynyl is preferably selected from ethyne, propyne, butyne, pentyne and hexyne; and/or the aryl is selected from phenyl, naphtyl, or anthracene; preferably is napthyl or phenyl; and/or the heterocyclyl is a heterocyclic ring system of one or more saturated or unsaturated rings of which at least one ring contains one or more heteroatoms from the group consisting of nitrogen, oxygen and/or sulfur in the ring; preferably is a heterocyclic ring system of one or two saturated or unsaturated rings of which at least one ring contains one or more heteroatoms from the group consisting of nitrogen, oxygen and/or sulfur in the ring, more preferably is selected from imidazole, oxadiazole, tetrazole, pyridine, pyrimidine, piperidine, piperazine, benzofuran, benzimidazole, indazole, benzothiazole, benzodiazole, thiazole, benzothiazole, tetrahydropyrane, morpholine, indoline, furan, triazole, isoxazole, pyrazole, thiophene, benzothiophene, pyrrole, pyrazine, pyrrolo[2,3b]pyridine, quinoline, isoquinoline, phthalazine, benzo-1,2,5-thiadiazole, indole, benzotriazole, benzoxazole oxopyrrolidine, pyrimidine, benzodioxolane, benzodioxane, carbazole and quinazoline; and/or the cycloalkyl is C₃₋₈ cycloalkyl like cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, cycloheptyl, or cyclooctyl; preferably is C₃₋₇ cycloalkyl like cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, or cycloheptyl; more preferably from C₃₋₆ cycloalkyl like cyclopropyl, cyclobutyl, cyclopentyl or cyclohexyl; more preferably the cycloalkyl is cyclopropyl; optionally in form of one of the stereoisomers, preferably enantiomers or diastereomers, a racemate or in form of a mixture of at least two of the stereoisomers, preferably enantiomers and/or diastereomers, in any mixing ratio, or a corresponding salt thereof, or a corresponding solvate thereof.

In another preferred embodiment of the invention according to general Formula (I) the compound is a compound, wherein in R₃ and R_(3′) are methyl.

In another preferred embodiment of the invention according to general Formula (I) the compound is a compound, wherein in R₃ and R_(3′) are hydrogen.

In another preferred embodiment of the invention according to general Formula (I) the compound is a compound, wherein in R₄ and R_(4′) as defined in any of the embodiments of the present invention,

the C₁₋₆ alkyl is preferably selected from methyl, ethyl, propyl, butyl, pentyl, hexyl, isopropyl and 2-methylpropyl; and/or the C₂₋₆-alkenyl is preferably selected from ethylene, propylene, butylene, pentylene and hexylene; and/or the C₂₋₆-alkynyl is preferably selected from ethyne, propyne, butyne, pentyne and hexyne; optionally in form of one of the stereoisomers, preferably enantiomers or diastereomers, a racemate or in form of a mixture of at least two of the stereoisomers, preferably enantiomers and/or diastereomers, in any mixing ratio, or a corresponding salt thereof, or a corresponding solvate thereof.

In another preferred embodiment of the invention according to general Formula (I) the compound is a compound, wherein in R₅ and R_(5′) as defined in any of the embodiments of the present invention,

the C₁₋₆ alkyl is preferably selected from methyl, ethyl, propyl, butyl, pentyl, hexyl, isopropyl and 2-methylpropyl; more preferably the C₁₋₆ alkyl is methyl; and/or the C₂₋₆-alkenyl is preferably selected from ethylene, propylene, butylene, pentylene and hexylene; and/or the C₂₋₆-alkynyl is preferably selected from ethyne, propyne, butyne, pentyne and hexyne; and/or the heterocyclyl is a heterocyclic ring system of one or more saturated or unsaturated rings of which at least one ring contains one or more heteroatoms from the group consisting of nitrogen, oxygen and/or sulfur in the ring; preferably is a heterocyclic ring system of one or two saturated or unsaturated rings of which at least one ring contains one or more heteroatoms from the group consisting of nitrogen, oxygen and/or sulfur in the ring, more preferably is selected from imidazole, oxadiazole, tetrazole, pyridine, pyrimidine, piperidine, piperazine, benzofuran, benzimidazole, indazole, benzothiazole, benzodiazole, thiazole, benzothiazole, tetrahydropyrane, morpholine, indoline, furan, triazole, isoxazole, pyrazole, thiophene, benzothiophene, pyrrole, pyrazine, pyrrolo[2,3b]pyridine, quinoline, isoquinoline, phthalazine, benzo-1,2,5-thiadiazole, indole, benzotriazole, benzoxazole oxopyrrolidine, pyrimidine, benzodioxolane, benzodioxane, carbazole and quinazoline; and/or the cycloalkyl is C₃₋₈ cycloalkyl like cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, cycloheptyl, or cyclooctyl; preferably is C₃₋₇ cycloalkyl like cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, or cycloheptyl; more preferably from C₃₋₆ cycloalkyl like cyclopropyl, cyclobutyl, cyclopentyl or cyclohexyl; optionally in form of one of the stereoisomers, preferably enantiomers or diastereomers, a racemate or in form of a mixture of at least two of the stereoisomers, preferably enantiomers and/or diastereomers, in any mixing ratio, or a corresponding salt thereof, or a corresponding solvate thereof.

In another preferred embodiment of the invention according to general Formula (I) the compound is a compound, wherein in R₆ and R_(6′) as defined in any of the embodiments of the present invention,

the C₁₋₆ alkyl is preferably selected from methyl, ethyl, propyl, butyl, pentyl, hexyl, isopropyl and 2-methylpropyl; more preferably the C₁₋₆ alkyl is methyl; and/or the C₂₋₆-alkenyl is preferably selected from ethylene, propylene, butylene, pentylene and hexylene; and/or the C₂₋₆-alkynyl is preferably selected from ethyne, propyne, butyne, pentyne and hexyne; optionally in form of one of the stereoisomers, preferably enantiomers or diastereomers, a racemate or in form of a mixture of at least two of the stereoisomers, preferably enantiomers and/or diastereomers, in any mixing ratio, or a corresponding salt thereof, or a corresponding solvate thereof.

In another preferred embodiment of the invention according to general Formula (I) the compound is a compound, wherein in R₇ as defined in any of the embodiments of the present invention,

the C₁₋₆ alkyl is preferably selected from methyl, ethyl, propyl, butyl, pentyl, hexyl, isopropyl and 2-methylpropyl; and/or the C₂₋₆-alkenyl is preferably selected from ethylene, propylene, butylene, pentylene and hexylene; and/or the C₂₋₆-alkynyl is preferably selected from ethyne, propyne, butyne, pentyne and hexyne; optionally in form of one of the stereoisomers, preferably enantiomers or diastereomers, a racemate or in form of a mixture of at least two of the stereoisomers, preferably enantiomers and/or diastereomers, in any mixing ratio, or a corresponding salt thereof, or a corresponding solvate thereof.

In another preferred embodiment of the invention according to general Formula (I) the compound is a compound, wherein in R₈ as defined in any of the embodiments of the present invention,

the C₁₋₆ alkyl is preferably selected from methyl, ethyl, propyl, butyl, pentyl, hexyl, isopropyl and 2-methylpropyl; and/or the C₂₋₆-alkenyl is preferably selected from ethylene, propylene, butylene, pentylene and hexylene; and/or the C₂₋₆-alkynyl is preferably selected from ethyne, propyne, butyne, pentyne and hexyne; optionally in form of one of the stereoisomers, preferably enantiomers or diastereomers, a racemate or in form of a mixture of at least two of the stereoisomers, preferably enantiomers and/or diastereomers, in any mixing ratio, or a corresponding salt thereof, or a corresponding solvate thereof.

In another preferred embodiment of the invention according to general Formula (I) the compound is a compound, wherein in R₁₁, R_(11′) and R_(11″) as defined in any of the embodiments of the present invention,

the C₁₋₆ alkyl is preferably selected from methyl, ethyl, propyl, butyl, pentyl, hexyl, isopropyl and 2-methylpropyl; and/or the C₂₋₆-alkenyl is preferably selected from ethylene, propylene, butylene, pentylene and hexylene; and/or the C₂₋₆-alkynyl is preferably selected from ethyne, propyne, butyne, pentyne and hexyne; optionally in form of one of the stereoisomers, preferably enantiomers or diastereomers, a racemate or in form of a mixture of at least two of the stereoisomers, preferably enantiomers and/or diastereomers, in any mixing ratio, or a corresponding salt thereof, or a corresponding solvate thereof.

In another preferred embodiment of the invention according to general Formula (I) the compound is a compound, wherein in R_(11′″) as defined in any of the embodiments of the present invention,

the C₁₋₆ alkyl is preferably selected from methyl, ethyl, propyl, butyl, pentyl, hexyl, isopropyl and 2-methylpropyl; and/or the C₂₋₆-alkenyl is preferably selected from ethylene, propylene, butylene, pentylene and hexylene; and/or the C₂₋₆-alkynyl is preferably selected from ethyne, propyne, butyne, pentyne and hexyne; optionally in form of one of the stereoisomers, preferably enantiomers or diastereomers, a racemate or in form of a mixture of at least two of the stereoisomers, preferably enantiomers and/or diastereomers, in any mixing ratio, or a corresponding salt thereof, or a corresponding solvate thereof.

In another preferred embodiment of the invention according to general Formula (I) the compound is a compound, wherein in R₁₂, R_(12′) and R_(12″) as defined in any of the embodiments of the present invention,

the C₁₋₆ alkyl is preferably selected from methyl, ethyl, propyl, butyl, pentyl, hexyl, isopropyl and 2-methylpropyl; and/or the C₂₋₆-alkenyl is preferably selected from ethylene, propylene, butylene, pentylene and hexylene; and/or the C₂₋₆-alkynyl is preferably selected from ethyne, propyne, butyne, pentyne and hexyne; optionally in form of one of the stereoisomers, preferably enantiomers or diastereomers, a racemate or in form of a mixture of at least two of the stereoisomers, preferably enantiomers and/or diastereomers, in any mixing ratio, or a corresponding salt thereof, or a corresponding solvate thereof.

In another preferred embodiment of the invention according to general Formula (I) the compound is a compound, wherein in R_(12′″) as defined in any of the embodiments of the present invention,

the C₁₋₆ alkyl is preferably selected from methyl, ethyl, propyl, butyl, pentyl, hexyl, isopropyl and 2-methylpropyl; and/or the C₂₋₆-alkenyl is preferably selected from ethylene, propylene, butylene, pentylene and hexylene; and/or the C₂₋₆-alkynyl is preferably selected from ethyne, propyne, butyne, pentyne and hexyne; optionally in form of one of the stereoisomers, preferably enantiomers or diastereomers, a racemate or in form of a mixture of at least two of the stereoisomers, preferably enantiomers and/or diastereomers, in any mixing ratio, or a corresponding salt thereof, or a corresponding solvate thereof.

In another preferred embodiment of the invention according to general Formula (I) the compound is a compound, wherein in R₁₃ and R_(13″″) as defined in any of the embodiments of the present invention,

the C₁₋₆ alkyl is preferably selected from methyl, ethyl, propyl, butyl, pentyl, hexyl, isopropyl and 2-methylpropyl; and/or the C₂₋₆-alkenyl is preferably selected from ethylene, propylene, butylene, pentylene and hexylene; and/or the C₂₋₆-alkynyl is preferably selected from ethyne, propyne, butyne, pentyne and hexyne; optionally in form of one of the stereoisomers, preferably enantiomers or diastereomers, a racemate or in form of a mixture of at least two of the stereoisomers, preferably enantiomers and/or diastereomers, in any mixing ratio, or a corresponding salt thereof, or a corresponding solvate thereof.

In another preferred embodiment of the invention according to general Formula (I) the compound is a compound, wherein in R₁₄, R_(14′) and R_(14″) as defined in any of the embodiments of the present invention,

the C₁₋₆ alkyl is preferably selected from methyl, ethyl, propyl, butyl, pentyl, hexyl, isopropyl and 2-methylpropyl; and/or the C₂₋₆-alkenyl is preferably selected from ethylene, propylene, butylene, pentylene and hexylene; and/or the C₂₋₆-alkynyl is preferably selected from ethyne, propyne, butyne, pentyne and hexyne; and/or the aryl is selected from phenyl, naphtyl and anthracene; preferably is napthyl or phenyl; and/or the heterocyclyl is a heterocyclic ring system of one or more saturated or unsaturated, rings of which at least one ring contains one or more heteroatoms from the group consisting of nitrogen, oxygen and/or sulfur in the ring; preferably is a heterocyclic ring system of one or two saturated or unsaturated rings of which at least one ring contains one or more heteroatoms from the group consisting of nitrogen, oxygen and/or sulfur in the ring, more preferably is selected from imidazole, oxadiazole, tetrazole, pyridine, pyrimidine, piperidine, piperazine, benzofuran, benzimidazole, indazole, benzothiazole, benzodiazole, thiazole, benzothiazole, tetrahydropyrane, morpholine, indoline, furan, triazole, isoxazole, pyrazole, thiophene, benzothiophene, pyrrole, pyrazine, pyrrolo[2,3b]pyridine, quinoline, isoquinoline, phthalazine, benzo-1,2,5-thiadiazole, indole, benzotriazole, benzoxazole oxopyrrolidine, pyrimidine, benzodioxolane, benzodioxane, carbazole and quinazoline; and/or the cycloalkyl is C₃₋₈ cycloalkyl like cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, cycloheptyl, or cyclooctyl; preferably is C₃₋₇ cycloalkyl like cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, or cycloheptyl; more preferably from C₃₋₆ cycloalkyl like cyclopropyl, cyclobutyl, cyclopentyl or cyclohexyl; optionally in form of one of the stereoisomers, preferably enantiomers or diastereomers, a racemate or in form of a mixture of at least two of the stereoisomers, preferably enantiomers and/or diastereomers, in any mixing ratio, or a corresponding salt thereof, or a corresponding solvate thereof.

In another preferred embodiment of the invention according to general Formula (I) the compound is a compound, wherein in R_(14′″) as defined in any of the embodiments of the present invention,

the C₁₋₆ alkyl is preferably selected from methyl, ethyl, propyl, butyl, pentyl, hexyl, isopropyl and 2-methylpropyl; and/or the C₂₋₆-alkenyl is preferably selected from ethylene, propylene, butylene, pentylene and hexylene; and/or the C₂₋₆-alkynyl is preferably selected from ethyne, propyne, butyne, pentyne and hexyne; optionally in form of one of the stereoisomers, preferably enantiomers or diastereomers, a racemate or in form of a mixture of at least two of the stereoisomers, preferably enantiomers and/or diastereomers, in any mixing ratio, or a corresponding salt thereof, or a corresponding solvate thereof.

In another preferred embodiment of the invention according to general Formula (I) the compound is a compound, wherein in R_(n) as defined in any of the embodiments of the present invention,

the C₁₋₆ alkyl is preferably selected from methyl, ethyl, propyl, butyl, pentyl, hexyl, isopropyl and 2-methylpropyl, preferably the C₁₋₆ alkyl is methyl; and/or the C₂₋₆-alkenyl is preferably selected from ethylene, propylene, butylene, pentylene and hexylene; and/or the C₂₋₆-alkynyl is preferably selected from ethyne, propyne, butyne, pentyne and hexyne; optionally in form of one of the stereoisomers, preferably enantiomers or diastereomers, a racemate or in form of a mixture of at least two of the stereoisomers, preferably enantiomers and/or diastereomers, in any mixing ratio, or a corresponding salt thereof, or a corresponding solvate thereof.

In another preferred embodiment of the invention according to general Formula (I) the compound is a compound, wherein in R_(x) as defined in any of the embodiments of the present invention,

the C₁₋₆ alkyl is preferably selected from methyl, ethyl, propyl, butyl, pentyl, hexyl, isopropyl and 2-methylpropyl; and/or the C₂₋₆-alkenyl is preferably selected from ethylene, propylene, butylene, pentylene and hexylene; and/or the C₂₋₆-alkynyl is preferably selected from ethyne, propyne, butyne, pentyne and hexyne; optionally in form of one of the stereoisomers, preferably enantiomers or diastereomers, a racemate or in form of a mixture of at least two of the stereoisomers, preferably enantiomers and/or diastereomers, in any mixing ratio, or a corresponding salt thereof, or a corresponding solvate thereof.

In another preferred embodiment of the invention according to general Formula (I) the compound is a compound, wherein in R_(x′) as defined in any of the embodiments of the present invention,

the C₁₋₆ alkyl is preferably selected from methyl, ethyl, propyl, butyl, pentyl, hexyl, isopropyl and 2-methylpropyl; and/or the C₂₋₆-alkenyl is preferably selected from ethylene, propylene, butylene, pentylene and hexylene; and/or the C₂₋₆-alkynyl is preferably selected from ethyne, propyne, butyne, pentyne and hexyne; optionally in form of one of the stereoisomers, preferably enantiomers or diastereomers, a racemate or in form of a mixture of at least two of the stereoisomers, preferably enantiomers and/or diastereomers, in any mixing ratio, or a corresponding salt thereof, or a corresponding solvate thereof.

In another preferred embodiment of the invention according to general Formula (I) the compound is a compound, wherein

R₁ is

optionally in form of one of the stereoisomers, preferably enantiomers or diastereomers, a racemate or in form of a mixture of at least two of the stereoisomers, preferably enantiomers and/or diastereomers, in any mixing ratio, or a corresponding salt thereof, or a corresponding solvate thereof.

In another preferred embodiment of the invention according to general Formula (I) the compound is a compound, wherein

R₁ is

optionally in form of one of the stereoisomers, preferably enantiomers or diastereomers, a racemate or in form of a mixture of at least two of the stereoisomers, preferably enantiomers and/or diastereomers, in any mixing ratio, or a corresponding salt thereof, or a corresponding solvate thereof.

In another preferred embodiment of the invention according to general Formula (I) the compound is a compound, wherein

-   -   R₁ is

and X is a bond; optionally in form of one of the stereoisomers, preferably enantiomers or diastereomers, a racemate or in form of a mixture of at least two of the stereoisomers, preferably enantiomers and/or diastereomers, in any mixing ratio, or a corresponding salt thereof, or a corresponding solvate thereof.

In another preferred embodiment of the invention according to any one of general Formulas (I′), (I^(a′)), (I^(b′)), (I^(2′)), (I^(3′)) or (I^(4′)) the compound is a compound, wherein

R₁ is

and optionally in form of one of the stereoisomers, preferably enantiomers or diastereomers, a racemate or in form of a mixture of at least two of the stereoisomers, preferably enantiomers and/or diastereomers, in any mixing ratio, or a corresponding salt thereof, or a corresponding solvate thereof.

In another preferred embodiment of the invention according to general Formula (I) the compound is a compound, wherein

n is 0, 1, 2, 3, 4 or 5; preferably n is 0, 1 or 2; optionally in form of one of the stereoisomers, preferably enantiomers or diastereomers, a racemate or in form of a mixture of at least two of the stereoisomers, preferably enantiomers and/or diastereomers, in any mixing ratio, or a corresponding salt thereof, or a corresponding solvate thereof.

In another preferred embodiment of the invention according to general Formula (I) the compound is a compound, wherein

m is 1, 2, 3, 4 or 5; preferably m is I or 2; optionally in form of one of the stereoisomers, preferably enantiomers or diastereomers, a racemate or in form of a mixture of at least two of the stereoisomers, preferably enantiomers and/or diastereomers, in any mixing ratio, or a corresponding salt thereof, or a corresponding solvate thereof.

In another preferred embodiment of the invention according to general Formula (I) the compound is a compound, wherein

p is 0, 1 or 2; preferably p is 0 or 1; optionally in form of one of the stereoisomers, preferably enantiomers or diastereomers, a racemate or in form of a mixture of at least two of the stereoisomers, preferably enantiomers and/or diastereomers, in any mixing ratio, or a corresponding salt thereof, or a corresponding solvate thereof.

In another preferred embodiment of the invention according to general Formula (I) the compound is a compound, wherein

X is a bond, —C(R_(x)R_(x′))—, —O—, —C(O)—, —C(O)NR₇—, —NR₇C(O)— or —C(O)O—; preferably, X is a bond: optionally in form of one of the stereoisomers, preferably enantiomers or diastereomers, a racemate or in form of a mixture of at least two of the stereoisomers, preferably enantiomers and/or diastereomers, in any mixing ratio, or a corresponding salt thereof, or a corresponding solvate thereof.

In another preferred embodiment of the invention according to general Formula (I) the compound is a compound, wherein

Y is —CH₂— or —C(O)—;

optionally in form of one of the stereoisomers, preferably enantiomers or diastereomers, a racemate or in form of a mixture of at least two of the stereoisomers, preferably enantiomers and/or diastereomers, in any mixing ratio, or a corresponding salt thereof, or a corresponding solvate thereof.

In a further preferred embodiment of the invention according to general Formula (I) the compound is a compound, wherein

X is a bond, —C(R_(x)R_(x′))—, —O—, —C(O)—, —C(O)NR₇—, —NR₇C(O)— or —C(O)O—; preferably X is a bond and/or m is 1, 2, 3, 4 or 5; preferably m is 1 or 2; and/or n is 0, 1, 2, 3, 4 or 5; preferably n is 0; and/or p is 0, 1 or 2; preferably p is 0; optionally in form of one of the stereoisomers, preferably enantiomers or diastereomers, a racemate or in form of a mixture of at least two of the stereoisomers, preferably enantiomers and/or diastereomers, in any mixing ratio, or a corresponding salt thereof, or a corresponding solvate thereof.

In another preferred embodiment of the invention according to general Formula (I) the compound is a compound, wherein

R₁ is

m is 1, or 2; n is 0; p is 0, or 1; X is a bond;

Y is —CH₂— or —C(O)—;

R₁ is selected from substituted or unsubstituted C₁₋₆ alkyl, substituted or unsubstituted cycloalkyl and substituted or unsubstituted aryl; R₂ is selected from hydrogen, substituted or unsubstituted C₁₋₆ alkyl, substituted or unsubstituted aryl and substituted or unsubstituted heterocyclyl; R₃ and R_(3′) taken together with the connecting C-atom form an substituted or unsubstituted cycloalkyl; R₄ and R_(4′) are hydrogen; R₅ and R_(5′) are independently selected from hydrogen and substituted or unsubstituted C₁₋₆ alkyl; R_(n) is selected from hydrogen and unsubstituted C₁₋₆ alkyl; optionally in form of one of the stereoisomers, preferably enantiomers or diastereomers, a racemate or in form of a mixture of at least two of the stereoisomers, preferably enantiomers and/or diastereomers, in any mixing ratio, or a corresponding salt thereof, or a corresponding solvate thereof.

Preferably, in this embodiment directly above the following additionally applies:

-   -   wherein said aryl in R_(1′) if substituted, is substituted with         one or more substituent/s selected from halogen, —R₁₁, —OR₁₁,         —NO₂, —NR₁₁R_(11′″), NR₁₁C(O)R_(11′), —NR₁₁S(O)₂R_(11′),         —S(O)₂NR₁₁R_(11′), —NR₁₁C(O)NR_(11′)R_(11″), —SR₁₁, —S(O)R₁₁,         S(O)₂R₁₁, —CN, haloalkyl, haloalkoxy, —C(O)OR₁₁,         —C(O)NR₁₁R_(11′), —OCH₂CH₂OH, —NR₁₁S(O)₂NR_(11′)R_(11″), and         C(CH)₂OR₁₁;     -   wherein the alkyl in R_(1′), if substituted, is substituted with         one or more substituent/s selected from —OR₁₁, halogen, —CN,         haloalkyl, haloalkoxy and —NR₁₁R_(11′″);     -   wherein R₁₁, R_(11′) and R_(11″) are independently selected from         hydrogen, unsubstituted C₁₋₆ alkyl, unsubstituted C₂₋₆ alkenyl         and unsubstituted C₂₋₆ alkynyl;         and wherein R_(11′″) is selected from hydrogen, unsubstituted         C₁₋₆ alkyl, unsubstituted C₂₋₆ alkenyl, unsubstituted C₂₋₆         alkynyl and -Boc;         and/or     -   wherein said aryl in R₂, if substituted, is substituted with one         or more substituent/s selected from halogen, —R₁₂, —OR₁₂, —NO₂,         —NR₁₂R_(12′″), NR₁₂C(O)R_(12′), —NR₁₂S(O)₂R_(12′),         —S(O)₂NR₁₂R_(12′), —NR₁₂C(O)NR_(12′)R_(12″), —SR₁₂, —S(O)R₁₂,         S(O)₂R₁₂, —CN, haloalkyl, haloalkoxy, —C(O)OR₂,         —C(O)NR₁₂R_(12′), —OCH₂CH₂OH, —NR₁₂S(O)₂NR_(12′)R_(12″) and         C(CH₃)₂OR₁₂;     -   additionally, cycloalkyl or non-aromatic heterocyclyl in R₂, if         substituted, may also be substituted with

or ═O;

-   -   wherein the alkyl in R₂, if substituted, is substituted with one         or more substituent/s selected from —OR₁₂, halogen, —CN,         haloalkyl, haloalkoxy and —NR₁₂R_(12′″);     -   wherein R₁₂, R_(12′) and R_(12″) are independently selected from         hydrogen, unsubstituted C₁₋₆ alkyl, unsubstituted C₂₋₆ alkenyl         and unsubstituted C₂₋₆ alkynyl;     -   and wherein R_(12′″) is selected from hydrogen, unsubstituted         C₁₋₆ alkyl, unsubstituted C₂₋₆ alkenyl, unsubstituted C₂₋₆         alkynyl and -Boc;         and/or         the alkyl, alkenyl or alkynyl, other than those defined in         R_(1′) or R₂, if substituted, is substituted with one or more         substituent/s selected from —OR₁₃, halogen, —CN, haloalkyl,         haloalkoxy and —NR₁₃R_(13′″);     -   wherein R₁₃ is selected from hydrogen, unsubstituted C₁₋₆ alkyl,         unsubstituted C₂₋₆ alkenyl, and unsubstituted C₂₋₆ alkynyl;     -   R_(13′″) is selected from hydrogen, unsubstituted C₁₋₆ alkyl,         unsubstituted C₂₋₆ alkenyl, unsubstituted C₂₋₆ alkynyl and -Boc;         the aryl, heterocyclyl or cycloalkyl other than those defined in         R_(1′) or R₂, if substituted, is substituted with one or more         substituent/s selected from halogen, —R₁₄, —OR₁₄, —NO₂,         —NR₁₄R_(14′″), NR₁₄C(O)R_(14′), —NR₁₄S(O)₂R_(14′),         —S(O)₂NR₁₄R₁₄, —NR₁₄C(O)NR_(14′)R_(14″), —SR₁₄, —S(O)R₁₄,         S(O)₂R₁₄, —CN, haloalkyl, haloalkoxy, —C(O)OR₁₄,         —C(O)NR₁₄R_(14′), —OCH₂CH₂OH, —NR₁₄S(O)₂NR_(14′)R_(14″) and         C(CH₃)₂OR₁₄;         additionally, wherein cycloalkyl or non-aromatic heterocyclyl,         other than those defined in R_(1′) or R₂, if substituted, may         also be substituted with

or ═O;

-   -   wherein R₁₄, R_(14′) and R_(14″) are independently selected from         hydrogen, unsubstituted C₁₋₆ alkyl, unsubstituted C₂₋₆ alkenyl,         unsubstituted C₂₋₆ alkynyl, unsubstituted aryl, unsubstituted         cycloalkyl and unsubstituted heterocyclyl;     -   and wherein R_(14′″) is selected from hydrogen, unsubstituted         C₁₋₆ alkyl, unsubstituted C₂₋₆ alkenyl, unsubstituted C₂₋₆         alkynyl and -Boc;

In another preferred embodiment of the invention according to general Formula (I), the compound is a compound of Formula (I′)

wherein R₁, R₂, R₃, R_(3′), R₅, R_(5′), R_(n), m and Y are as described above or as described below.

In another preferred embodiment of the invention according to general Formula (I), the compound is a compound of Formula (I′)

wherein

R₁ is or

m is 1,2,3, 4 or 5; p is 0, 1 or 2;

Y is —CH₂— or —C(O)—;

X is a bond, —C(R_(x)R_(x′))—, —O—, —C(O)—, —C(O)NR₇—, —NR₇C(O)— or —C(O)O—;

-   -   wherein R_(x) is selected from halogen, —OR₇, substituted or         unsubstituted C₁₋₆ alkyl, substituted or unsubstituted C₂₋₆         alkenyl and substituted or unsubstituted C₂₋₆ alkynyl;     -   R_(x′) is selected from hydrogen, halogen, substituted or         unsubstituted C₁₋₆ alkyl, substituted or unsubstituted C₂₋₆         alkenyl and substituted or unsubstituted C₂₋₆ alkynyl;     -   R₇ is selected from hydrogen, substituted or unsubstituted C₁₋₆         alkyl, substituted or unsubstituted C₂₋₆ alkenyl and substituted         or unsubstituted C₂₋₆ alkynyl;         R_(1′) is selected from substituted or unsubstituted C₁₋₆ alkyl,         substituted or unsubstituted C₂₋₆ alkenyl, substituted or         unsubstituted C₂₋₆ alkynyl, substituted or unsubstituted         cycloalkyl, substituted or unsubstituted aryl and substituted or         unsubstituted heterocyclyl;         R₂ is selected from hydrogen, substituted or unsubstituted C₁₋₆         alkyl, substituted or unsubstituted C₂₋₆ alkenyl, substituted or         unsubstituted C₂₋₆ alkynyl, substituted or unsubstituted         cycloalkyl, substituted or unsubstituted aryl and substituted or         unsubstituted heterocyclyl;         R₃ and R_(3′) are independently selected from hydrogen,         substituted or unsubstituted C₁₋₆ alkyl, substituted or         unsubstituted C₂₋₆ alkenyl, substituted or unsubstituted C₂₋₆         alkynyl, substituted or unsubstituted cycloalkyl, substituted or         unsubstituted alkylcycloalkyl, substituted or unsubstituted         alkylaryl, substituted or unsubstituted aryl, substituted or         unsubstituted heterocyclyl or substituted or unsubstituted         alkylheterocyclyl;         alternatively R₃ and R_(3′) taken together with the connecting         C-atom may form an substituted or unsubstituted cycloalkyl;         R₄ and R_(4′) are independently selected from hydrogen,         substituted or unsubstituted C₁₋₆ alkyl, substituted or         unsubstituted C₂₋₆ alkenyl and substituted or unsubstituted C₂₋₆         alkynyl;         R₅ and R_(5′) are independently selected from hydrogen,         substituted or unsubstituted C₁₋₆ alkyl, substituted or         unsubstituted C₂₋₆ alkenyl and substituted or unsubstituted C₂₋₆         alkynyl;         alternatively, R₅ and R_(5′) taken together with the connecting         C-atom may form an substituted or unsubstituted cycloalkyl or a         substituted or unsubstituted heterocyclyl;         R_(n) is selected from hydrogen, unsubstituted C₁₋₆ alkyl,         unsubstituted C₂₋₆ alkenyl and unsubstituted C₂₋₆ alkynyl;         optionally in form of one of the stereoisomers, preferably         enantiomers or diastereomers, a racemate or in form of a mixture         of at least two of the stereoisomers, preferably enantiomers         and/or diastereomers, in any mixing ratio, or a corresponding         salt thereof, or a corresponding solvate thereof.

In a further preferred embodiment of the invention according to general Formula (I) the compound is a compound of Formula (I²),

wherein R₁, R₂, R₅, R_(5′), R_(n), m and Y are as described above or as described below.

In a further preferred embodiment of the invention according to general Formula (I) the compound is a compound of Formula (I^(2′)),

wherein

R₁ is

m is 1, 2, 3, 4 or 5; p is 0, 1 or 2;

Y is —CH₂— or —C(O)—;

X is a bond, —C(R_(x)R_(x′))—, —O—, —C(O)—, —C(O)NR₇—, —NR₇C(O)— or —C(O)O—;

-   -   wherein R_(x) is selected from halogen, —OR₇, substituted or         unsubstituted C₁₋₆ alkyl, substituted or unsubstituted C₂₋₆         alkenyl and substituted or unsubstituted C₂₋₆ alkynyl;     -   R_(x′) is selected from hydrogen, halogen, substituted or         unsubstituted C₁₋₆ alkyl, substituted or unsubstituted C₂₋₆         alkenyl and substituted or unsubstituted C₂₋₆ alkynyl;     -   R₇ is selected from hydrogen, substituted or unsubstituted C₁₋₆         alkyl, substituted or unsubstituted C₂₋₆ alkenyl and substituted         or unsubstituted C₂₋₆ alkynyl;         R_(1′) is selected from, substituted or unsubstituted C₁₋₆,         alkyl, substituted or unsubstituted C₂₋₆ alkenyl, substituted or         unsubstituted C₂₋₆ alkynyl, substituted or unsubstituted         cycloalkyl, substituted or unsubstituted aryl and substituted or         unsubstituted heterocyclyl;         R₂ is selected from hydrogen, substituted or unsubstituted C₁₋₆         alkyl, substituted or unsubstituted C₂₋₆ alkenyl, substituted or         unsubstituted C₂₋₆ alkynyl, substituted or unsubstituted         cycloalkyl, substituted or unsubstituted aryl and substituted or         unsubstituted heterocyclyl;         R₄ and R_(4′) are independently selected from hydrogen,         substituted or unsubstituted C₁₋₆ alkyl, substituted or         unsubstituted C₂₋₆ alkenyl and substituted or unsubstituted C₂₋₆         alkynyl;         R₅ and R_(5′) are independently selected from hydrogen,         substituted or unsubstituted C₁₋₆ alkyl, substituted or         unsubstituted C₂₋₆ alkenyl and substituted or unsubstituted C₂₋₆         alkynyl;         alternatively, R₅ and R_(5′) taken together with the connecting         C-atom may form an substituted or unsubstituted cycloalkyl or a         substituted or unsubstituted heterocyclyl;         R_(n) is selected from hydrogen, unsubstituted C₁₋₆ alkyl,         unsubstituted C₂₋₆ alkenyl and unsubstituted C₂₋₆ alkynyl;         optionally in form of one of the stereoisomers, preferably         enantiomers or diastereomers, a racemate or in form of a mixture         of at least two of the stereoisomers, preferably enantiomers         and/or diastereomers, in any mixing ratio, or a corresponding         salt thereof, or a corresponding solvate thereof.

In a further preferred embodiment of the invention according to general Formula (I) the compound is a compound of Formula (I^(3′)),

wherein R_(1′), R₂, R₅, R_(5′), R_(n), m and Y are as described above or as described below.

In a further preferred embodiment of the invention according to general Formula (I) the compound is a compound of Formula (I^(3′)),

wherein m is 1,2,3, 4 or 5; p is 0, 1 or 2;

Y is —CH₂— or —C(O)—;

X is a bond, —C(R_(x)R_(x′))—, —O—, —C(O)—, —C(O)NR₇—, —NR₇C(O)— or —C(O)O;

-   -   wherein R_(x) is selected from halogen, —OR₇, substituted or         unsubstituted C₁₋₆ alkyl, substituted or unsubstituted C₂₋₆         alkenyl and substituted or unsubstituted C₂₋₆ alkynyl;     -   R_(x′) is selected from hydrogen, halogen, substituted or         unsubstituted C₁₋₆ alkyl, substituted or unsubstituted C₂₋₆         alkenyl and substituted or unsubstituted C₂₋₆ alkynyl;     -   R₇ is selected from hydrogen, substituted or unsubstituted C₁₋₆         alkyl, substituted or unsubstituted C₂₋₆ alkenyl and substituted         or unsubstituted C₂₋₆ alkynyl;         R_(1′) is selected from substituted or unsubstituted C₁₋₆ alkyl,         substituted or unsubstituted C₂₋₆ alkenyl, substituted or         unsubstituted C₂₋₆ alkynyl, substituted or unsubstituted         cycloalkyl, substituted or unsubstituted aryl and substituted or         unsubstituted heterocyclyl;         R₂ is selected from hydrogen, substituted or unsubstituted C₁₋₆         alkyl, substituted or unsubstituted C₂₋₆ alkenyl, substituted or         unsubstituted C₂₋₆ alkynyl, substituted or unsubstituted         cycloalkyl, substituted or unsubstituted aryl and substituted or         unsubstituted heterocyclyl;         R₄ and R_(4′) are independently selected from hydrogen,         substituted or unsubstituted C₁₋₆ alkyl, substituted or         unsubstituted C₂₋₆ alkenyl and substituted or unsubstituted C₂₋₆         alkynyl;         R₅ and R_(5′) are independently selected from hydrogen,         substituted or unsubstituted C₁₋₆ alkyl, substituted or         unsubstituted C₂₋₆ alkenyl and substituted or unsubstituted C₂₋₆         alkynyl;         alternatively, R₅ and R_(5′) taken together with the connecting         C-atom may form an substituted or unsubstituted cycloalkyl or a         substituted or unsubstituted heterocyclyl;         R_(n) is selected from hydrogen, unsubstituted C₁₋₆ alkyl,         unsubstituted C₂₋₆ alkenyl and unsubstituted C₂₋₆ alkynyl;         optionally in form of one of the stereoisomers, preferably         enantiomers or diastereomers, a racemate or in form of a mixture         of at least two of the stereoisomers, preferably enantiomers         and/or diastereomers, in any mixing ratio, or a corresponding         salt thereof, or a corresponding solvate thereof.

In a preferred embodiment

R₁ is a substituted or unsubstituted group selected from ethyl and phenyl.

In a preferred embodiment

R_(1′) is a substituted or unsubstituted group selected from methyl, ethyl and phenyl.

In a preferred embodiment

R₂ is hydrogen or a substituted or unsubstituted group selected from isopropyl, isobutyl and phenyl; more preferably hydrogen or an unsubstituted group selected from isopropyl, isobutyl and phenyl.

In a preferred embodiment

R₃ and R_(3′) taken together with the connecting C-atom may form a substituted or unsubstituted cyclopropyl: preferably unsubstituted cyclopropyl.

In a preferred embodiment

R₃ is substituted or unsubstituted methyl, preferably unsubstituted methyl.

In a preferred embodiment

R_(3′) is substituted or unsubstituted methyl, preferably unsubstituted methyl. In a preferred embodiment R₃ is hydrogen.

In a preferred embodiment

R_(3′) is hydrogen.

In a preferred embodiment

R₃ is substituted or unsubstituted methyl, preferably unsubstituted methyl, while R_(3′) is substituted or unsubstituted methyl, preferably unsubstituted methyl.

In a preferred embodiment

R₃ and R₃ are both substituted or unsubstituted methyl, preferably unsubstituted methyl.

In a preferred embodiment

R₃ and R₃ are both hydrogen.

In a preferred embodiment

R₄ and R_(4′) are both hydrogen.

In a preferred embodiment

R₅ is hydrogen or substituted or unsubstituted methyl, preferably R₅ is hydrogen or unsubstituted methyl.

In a preferred embodiment

R_(5′) is hydrogen.

In a preferred embodiment

R₅ is hydrogen or substituted or unsubstituted methyl, while R_(5′) is hydrogen, preferably R₅ is hydrogen or unsubstituted methyl, while R_(5′) is hydrogen.

In a preferred embodiment

R₅ is substituted or unsubstituted methyl, while R_(5′) is hydrogen, preferably R₅ is unsubstituted methyl, while R_(5′) is hydrogen.

In a preferred embodiment

R₅ and R_(5′) are both hydrogen.

In a preferred embodiment

R₆ is hydrogen or substituted or unsubstituted methyl, preferably R₆ is hydrogen or unsubstituted methyl.

In a preferred embodiment

R_(6′) is hydrogen.

In a preferred embodiment

R₆ is hydrogen or substituted or unsubstituted methyl, while R_(6′) is hydrogen, preferably R₆ is hydrogen or unsubstituted methyl, while R_(6′) is hydrogen.

In a preferred embodiment

R₆ is substituted or unsubstituted methyl, while R_(6′) is hydrogen, preferably R₆ is unsubstituted methyl, while R_(6′) is hydrogen.

In a preferred embodiment

R₆ and R_(6′) are both hydrogen.

In a preferred embodiment

R_(n) is hydrogen or substituted or unsubstituted methyl, preferably hydrogen or unsubstituted methyl.

In a preferred embodiment

X is a bond.

In a preferred embodiment

Y is —CH₂— or —C(O)—;

In another preferred embodiment

n is 0.

In another preferred embodiment

m is 1 or 2;

In another preferred embodiment

p is 0 or 1.

In another preferred embodiment

p is 0.

In an particular embodiment

the halogen is fluorine or chlorine.

In a preferred further embodiment, the compounds of the general Formula (I) are selected from

EX CHEMICAL NAME 1 (5s,8s)-8-(benzylamino)-12-ethyl-4-oxa-12- azadispiro[2.1.5.3]tridecan-13-one 2 (5r,8r)-8-(benzylamino)-12-ethyl-4-oxa-12- azadispiro[2.1.5.3]tridecan-13-one 3 (5s,8s)-12-ethyl-8-[methyl(2-phenylethyl)amino]-4-oxa-12- azadispiro[2.1.5.3]tridecan-13-one 4 (5r,8r)-12-ethyl-8-[methyl(2-phenylethyl)amino]-4-oxa-12- azadispiro[2.1.5.3]tridecan-13-one 5 (5s,8s)-8-[benzyl(methyl)amino]-12-ethyl-4-oxa-12- azadispiro[2.1.5.3]tridecan-13-one 6 (5s,8s)-12-ethyl-8-[(2-phenylethyl)amino]-4-oxa-12- azadispiro[2.1.5.3]tridecan-13-one 7 (5r,8r)-12-ethyl-8-[(2-phenylethyl)amino]-4-oxa-12- azadispiro[2.1.5.3]tridecan-13-one 8 (5s,8s)-8-[benzyl(methyl)amino]-12-phenyl-4-oxa-12- azadispiro[2.1.5.3]tridecan-13-one 9 (5s,8s)-8-[methyl(2-phenylethyl)amino]-12-phenyl-4-oxa-12- azadispiro[2.1.5.3]tridecan-13-one 10 (5s,8s)-8-(benzylamino)-12-phenyl-4-oxa-12- azadispiro[2.1.5.3]tridecan-13-one 11 (5s,8s)-12-phenyl-8-[(2-phenylethyl)amino]-4-oxa-12- azadispiro[2.1.5.3]tridecan-13-one 12 (5r,8r)-8-(benzylamino)-12-phenyl-4-oxa-12- azadispiro[2.1.5.3]tridecan-13-one 13 (5r,8r)-12-phenyl-8-[(2-phenylethyl)amino]-4-oxa-12- azadispiro[2.1.5.3]tridecan-13-one 14 (5r,8r)-8-[benzyl(methyl)amino]-12-phenyl-4-oxa-12- azadispiro[2.1.5.3]tridecan-13-one 15 (5r,8r)-8-[methyl(2-phenylethyl)amino]-12-phenyl-4-oxa-12- azadispiro[2.1.5.3]tridecan-13-one 16 (5r,8r)-8-[benzyl(methyl)amino]-12-ethyl-4-oxa-12- azadispiro[2.1.5.3]tridecan-13-one 17 (5s,8s)-N-benzyl-12-ethyl-N-methyl-4-oxa-12- azadispiro[2.1.5.3]tridecan-8-amine 18 (5r,8r)-N-benzyl-12-ethyl-N-methyl-4-oxa-12- azadispiro[2.1.5.3]tridecan-8-amine 19 (5s,8s)-N-benzyl-N-methyl-12-phenyl-4-oxa-12- azadispiro[2.1.5.3]tridecan-8-amine 20 (5r,8r)-N-benzyl-N-methyl-12-phenyl-4-oxa-12- azadispiro[2.1.5.3]tridecan-8-amine 21 (5r,8r)-12-ethyl-8-(methylamino)-4-oxa-12- azadispiro[2.1.5.3]tridecan-13-one acetate 22 (5s,8s)-12-ethyl-8-(methylamino)-4-oxa-12- azadispiro[2.1.5.3]tridecan-13-one acetate 23 (5s,8s)-8-(methylamino)-12-phenyl-4-oxa-12- azadispiro[2.1.5.3]tridecan-13-one acetate 24 (5r,8r)-8-(methylamino)-12-phenyl-4-oxa-12- azadispiro[2.1.5.3]tridecan-13-one acetate 25 (5s,8s)-N-methyl-12-phenyl-4-oxa-12- azadispiro[2.1.5.3]tridecan-8-amine acetate 26 (5r,8r)-N-methyl-12-phenyl-4-oxa-12-azadispiro[2.1.5.3]tridecan-8- amine acetate 27 (5r,8r)-12-ethyl-8-[methyl(3-methylbutyl)amino]-4-oxa-12- azadispiro[2.1.5.3]tridecan-13-one 28 (5s,8s)-12-ethyl-8-[methyl(3-methylbutyl)amino]-4-oxa-12- azadispiro[2.1.5.3]tridecan-13-one 29 (5s,8s)-8-[methyl(3-methylbutyl)amino]-12-phenyl-4-oxa-12- azadispiro[2.1.5.3]tridecan-13-one 30 (5r,8r)-8-[methyl(3-methylbutyl)amino]-12-phenyl-4-oxa-12- azadispiro[2.1.5.3]tridecan-13-one 31 (5s,8s)-N-methyl-N-(3-methylbutyl)-12-phenyl-4-oxa-12- azadispiro[2.1.5.3]tridecan-8-amine 32 (5r,8r)-N-methyl-N-(3-methylbutyl)-12-phenyl-4-oxa-12- azadispiro[2.1.5.3]tridecan-8-amine 33 (5s,8s)-12-ethyl-8-[methyl(2-methylpropyl)amino]-4-oxa-12- azadispiro[2.1.5.3]tridecan-13-one 34 (5r,8r)-N-methyl-12-phenyl-N-(2-phenylethyl)-4-oxa-12- azadispiro[2.1.5.3]tridecan-8-amine 35 (5r,8r)-12-ethyl-N-methyl-N-(3-methylbutyl)-4-oxa-12- azadispiro[2.1.5.3]tridecan-8-amine stereoisomers, preferably enantiomers and/or diastereomers, in any mixing ratio, or a corresponding salt thereof, or a corresponding solvate thereof.

In a preferred further embodiment, the compounds of the general Formula (I) are selected from

EX Structure Chemical name 36

(6s,9s)-9-(benzylamino)-4- ethyl-1-oxa-4- azaspiro[5.5]undecan-3- one 37

(6s,9r)-9-(benzylamino)-4- ethyl-oxa-4- azaspiro[5.5]undecan-3- one 38

(6s,9s)-4-ethyl-9- (isobutyl(methyl)amino)-1- oxa-4- azaspiro[5.5]undecan-3- one 39

(6s,9s)-9-(benzylamino)-4- ethyl-2,2-dimethyl-1-oxa- 4-azaspiro[5.5]undecan-3- one 40

(6s,9s)-9-(benzylamino)-4- ethyl-2,2-dimethyl-1-oxa- 4-azaspiro[5.5]undecan-3- one 41

(6s,9s)- (benzyl(methyl)amino)-4- ethyl-1-oxa-4- azaspiro[5.5]undecan-3- one 42

(6r,9r)-9- (benzyl(methyl)amino)-4- ethyl-1-oxa-4- azaspiro[5.5]undecan-3- one 43

(6s,9s)-9- (benzyl(methyl)amino)-4- ethyl-2,2-dimethyl-1-oxa- 4-azaspiro[5.5]undecan-3- one 44

(6r,9r)-9- (benzyl(methy)amino)-4- ethyl-2,2-dimethyl-1-oxa- 4-azaspiro[5.5]undecan-3- one 45

((5s,8s)-8- [Benzyl(methyl)amino]-4- oxa-12- azadispiro[2.1.5.3]tridecan- 12-yl)(phenyl)methanone 46

((5r,8s)-8- [Benzyl(methyl)amino]-4- oxa-12- azadispiro[2,1.5.3]tridecan- 12-yl)(phenyl)methanone 47

(6s-9s)-4-ethyl-9- (methylamino)-1-oxa-4- azasoiro[5.5]undecan-3- one acetate 48

(6s,9s)-4-ethyl-2,2- dimethyl-9-(methylamino)- 1-oxa-4- azaspiro[5.5]undecan-3- one acetate 49

(6r,9r)-4-ethyl-2,2- dimethyl-9-(methylamino)- 1-oxa-4- azaspiro[5.5]undecan-3- one acetate 50

((5s,8s)-8-(methylamino)- 4-oxa-12- azadispiro[2.1.5.3]tridecan- 12-yl)(phenyl)methanone acetate 51

(6s,9s)-4-ethyl-9- (methyl(phenethyl)amino- 1-oxa-4- azaspiro[5.5]undecan-3-one 52

(6s,9s)-4-ethyl-9- (isopentyl(methyl)amino)- 1-oxa-4- azaspiro[5.5]undecan-3- one 53

(6s,9s)-4-ethyl-9- (isopentyl(methyl)amino)- 2,2-dimethyl-1-oxa-4- azaspiro[5.5]undecan-3-one 54

(6s,9s)-4-ethyl-9- (isobutyl(methyl)amino)- 2,2-dimethyl-1-oxa-4- azaspiro[5.5]undecen-3- one 55

(6s,9s)-4-ethyl-2,2- dimethyl-9- (methyl(phenethyl)amino)- 1-oxa-4- azaspiro[5.5]undecan-3- one 56

(6r,9r)-4-ethyl-2,2- dimethyl-9- (methyl(phenelthyl)amino)- 1-oxa-4- azaspiro[5.5]undecan-3- one 57

(6r,9r)-4-ethyl-9- (isopentyl(methyl)amino)- 2,2-dimethyl-1-oxa-4- azaspiro[5.5]undecan-3- one 58

((5s,8s)-8- [methyl(phenethyl)amino]- 4-oxa-12- azadispiro[2.1.5.3]tridecan- 12-yl)(phenyl)methanone 59

((5s,8s)-8- [isopentyl(methyl)amino]- 4-oxa-12- azadispiro[2.1.5.3]tridecan- 12-yl)(phenyl)methanone 60

((5s,6s)-8- [isobutyl(methyl)amino]-4- oxa-12- azadispiro[2.1.5.3]tridecan- 12-yl)(phenyl)methanone 61

(6s,9s)-4-ethyl-N-methyl- N-phenethyl-1-oxa-4- azaspiro[5.5]undecan-9- amine 62

(6s,9s)-N-benzyl-4-ethyl- N,2,2-trimethyl-1-oxa-4- azespiro[5.5]undecan-9- amine 63

(6s,9s)-4-ethyl-N- isopentyl-N-methyl-1-oxa- 4-azaspiro[5.5]undecan-9- amine 64

(6s,9s)-4-ethyl-N- isopentyl-N,2,2-trimethyl- 1-oxa-4- azaspiro[5.5]underan-9- amine 65

(6s,9s)-4-ethyl-N-isobutyl- N,2,2-trinnethyl-1-oxa-4- azaspiro[5.5]undecan-9- amine 66

(6s,9s)-4-ethyl-N,2,2- trimethyl-N-phenethyl-1- oxa-4- azaspro[5.5]undecan-9- amine 67

(5s,8s)-12-benzyl-N- methyl-N-(2-phenylethyl)- 4-oxa-12- azadispiro[2.1.5.3]tridecan- 8-amine 68

(5s,8s)-12-benzyl-N- isobutyl-N-methyl-4-oxa- 12- azadispiro[2.1.5.3]tridecan- 8-amine optionally in form of one of the stereoisomers, preferably enantiomers or diastereomers, a racemate or in form of a mixture of at least two of the stereoisomers, preferably enantiomers and/or diastereomers, in any mixing ratio, or a corresponding salt thereof, or a corresponding solvate thereof.

In a preferred embodiment of the compound according to the invention of general Formula (I),

R_(1′) is selected from substituted or unsubstituted C₁₋₆ alkyl, substituted or unsubstituted C₂₋₆ alkenyl, substituted or unsubstituted C₂₋₆ alkynyl, substituted or unsubstituted cycloalkyl, substituted or unsubstituted aryl and substituted or unsubstituted heterocyclyl;

-   -   wherein said cycloalkyl, aryl or heterocyclyl in R_(1′) if         substituted, is substituted with one or more substituent/s         selected from halogen, —R₁₁, —OR₁₁, —NO₂, —NR₁₁R_(11′″),         NR₁₁C(O)R_(11′), —NR₁₁S(O)₂R_(11′), —S(O)₂NR₁₁R_(11′),         —NR₁₁C(O)NR_(11′)R_(11″), —SR₁₁, —S(O)R₁₁, S(O)₂R₁₁, —CN,         haloalkyl, haloalkoxy, —C(O)OR₁₁, —C(O)NR₁₁R_(11′), —OCH₂CH₂OH,         —NR₁₁S(O)₂NR_(11′)R_(11″) and C(CH₃)₂OR₁₁;     -   additionally, cycloalkyl or non-aromatic heterocyclyl in R_(1′),         if substituted, may also be substituted with

or ═O;

-   -   wherein the alkyl, alkenyl or alkynyl in R_(1′), if substituted,         is substituted with one or more substituent/s selected from         —OR₁₁, halogen, —CN, haloalkyl haloalkoxy and —NR₁₁R_(11′″);     -   wherein R₁₁, R_(11′) and R_(11″) are independently selected from         hydrogen, unsubstituted C₁₋₆ alkyl, unsubstituted C₂₋₆ alkenyl         and unsubstituted C₂₋₆ alkynyl;     -   and wherein R_(11′″) is selected from hydrogen, unsubstituted         C₁₋₆ alkyl, unsubstituted C₂₋₆ alkenyl, unsubstituted C₂₋₆         alkynyl and -Boc;         optionally in form of one of the stereoisomers, preferably         enantiomers or diastereomers, a racemate or in form of a mixture         of at least two of the stereoisomers, preferably enantiomers         and/or diastereomers, in any mixing ratio, or a corresponding         salt thereof, or a corresponding solvate thereof.

In another embodiment of the invention the compound of general Formula (I),

R₂ is selected from hydrogen, substituted or unsubstituted C₁₋₆ alkyl, substituted or unsubstituted C₂₋₆ alkenyl, substituted or unsubstituted C₂₋₆ alkynyl, substituted or unsubstituted cycloalkyl, substituted or unsubstituted aryl and substituted or unsubstituted heterocyclyl;

-   -   wherein said cycloalkyl, aryl or heterocyclyl in R₂, if         substituted, is substituted with one or more substituent/s         selected from halogen, —R₁₂, —OR₁₂, —NO₂, —NR₁₂R_(12′″),         NR₁₂C(O)R_(12′), —NR₁₂S(O)₂R_(12′), —S(O)₂NR₁₂R_(12′),         —NR₁₂C(O)NR_(12′)R_(12″), —SR₁₂, —S(O)R₁₂, S(O)₂R₁₂, —CN,         haloalkyl, haloalkoxy, —C(O)OR₁₂, —C(O)NR₁₂R_(12′), —OCH₂CH₂OH,         —NR₁₂S(O)₂NR_(12′)R_(12″) and C(CH₃)₂OR₁₂;     -   additionally, cycloalkyl or non-aromatic heterocyclyl in R₂, if         substituted, may also be substituted with

or ═O;

-   -   wherein the alkyl, alkenyl or alkynyl in R₂, if substituted, is         substituted with one or more substituent/s selected from —OR₁₂,         halogen, —CN, haloalkyl, haloalkoxy and —NR₁₂R_(12′″);     -   wherein R₁₂, R_(12′) and R_(12″) are independently selected from         hydrogen, unsubstituted C₁₋₆ alkyl, unsubstituted C₂₋₆ alkenyl         and unsubstituted C₂₋₆ alkynyl;     -   and wherein R_(12′″) is selected from hydrogen, unsubstituted         C₁₋₆ alkyl, unsubstituted C₂₋₆ alkenyl, unsubstituted C₂₋₆         alkynyl and -Boc;         optionally in form of one of the stereoisomers, preferably         enantiomers or diastereomers, a racemate or in form of a mixture         of at least two of the stereoisomers, preferably enantiomers         and/or diastereomers, in any mixing ratio, or a corresponding         salt thereof, or a corresponding solvate thereof.

In another embodiment of the invention the compound of general Formula (I),

the alkyl, alkenyl or alkynyl, other than those defined in R_(1′) or R₂, if substituted, is substituted with one or more substituent/s selected from —OR₁₃, halogen, —CN, haloalkyl, haloalkoxy and —NR₁₃R_(13′″);

-   -   wherein R₁₃ is selected from hydrogen, unsubstituted C₁₋₆ alkyl,         unsubstituted C₂₋₆ alkenyl, and unsubstituted C₂₋₆ alkynyl;     -   R_(13′″) is selected from hydrogen, unsubstituted C₁₋₆ alkyl,         unsubstituted C₂₋₆ alkenyl, unsubstituted C₂₋₆ alkynyl and -Boc;         optionally in form of one of the stereoisomers, preferably         enantiomers or diastereomers, a racemate or in form of a mixture         of at least two of the stereoisomers, preferably enantiomers         and/or diastereomers, in any mixing ratio, or a corresponding         salt thereof, or a corresponding solvate thereof.

In another embodiment of the invention the compound of general Formula (I),

the aryl, heterocyclyl or cycloalkyl other than those defined in R_(1′) or R₂, if substituted, is substituted with one or more substituent/s selected from halogen, —R₁₄, —OR₁₄, —NO₂, —NR₁₄R_(14′″), NR₁₄C(O)R_(14′), —NR₁₄S(O)₂R_(14′), —S(O)₂NR₁₄R_(14′), —NR₁₄C(O)NR_(14′)R₁₄″, —SR₁₄, —S(O)R₁₄, S(O)₂R₁₄, —CN, haloalkyl, haloalkoxy, —C(O)R₁₄, —C(O)NR₁₄R_(14′), —OCH₂CH₂OH, —NR₁₄S(O)₂NR_(14′)R_(14″) and C(CH₃)₂OR₁₄; additionally, wherein cycloalkyl or non-aromatic heterocyclyl, other than those defined in R_(1′) or R₂, if substituted, may also be substituted with

or ═O;

-   -   wherein R₁₄, R_(14′) and R_(14″) are independently selected from         hydrogen, unsubstituted C₁₋₆ alkyl, unsubstituted C₂₋₆ alkenyl,         unsubstituted C₂₋₆ alkynyl, unsubstituted aryl, unsubstituted         cycloalkyl and unsubstituted heterocyclyl;     -   and wherein R_(14′″) is selected from hydrogen, unsubstituted         C₁₋₆ alkyl, unsubstituted C₂₋₆ alkenyl, unsubstituted C₂₋₆         alkynyl and -Boc;         optionally in form of one of the stereoisomers, preferably         enantiomers or diastereomers, a racemate or in form of a mixture         of at least two of the stereoisomers, preferably enantiomers         and/or diastereomers, in any mixing ratio, or a corresponding         salt thereof, or a corresponding solvate thereof.         In a preferred embodiment of the compound according to the         invention of general Formula (I) and in relation to R_(1′) of         any of the embodiments of the present invention,     -   the cycloalkyl, aryl or heterocyclyl in R_(1′) if substituted,         is substituted with one or more substituent/s selected from         halogen, —R₁₁, —OR₁₁, —NO₂, —NR₁₁R_(11′″), NR₁₁C(O)R_(11′),         —NR₁₁S(O)₂R_(11′), —S(O)₂N₁₁R_(11′), —NR₁₁C(O)NR_(11′)R_(11″),         —SR₁₁, —S(O)R₁₁, S(O)₂R₁₁, —CN, haloalkyl haloalkoxy, —C(O)OR₁₁,         —C(O)NR₁₁R_(11′), —OCH₂CH₂OH, —NR₁₁S(O)₂NR_(11′)R_(11″), and         C(CH₃)OR₁₁;         optionally in form of one of the stereoisomers, preferably         enantiomers or diastereomers, a racemate or in form of a mixture         of at least two of the stereoisomers, preferably enantiomers         and/or diastereomers, in any mixing ratio, or a corresponding         salt thereof, or a corresponding solvate thereof.

In a preferred embodiment of the compound according to the invention of general Formula (I) and in relation to R_(1′) of any of the embodiments of the present invention,

-   -   the cycloalkyl or non-aromatic heterocyclyl in R_(1′) if         substituted, may also be substituted with

or ═O;

optionally in form of one of the stereoisomers, preferably enantiomers or diastereomers, a racemate or in form of a mixture of at least two of the stereoisomers, preferably enantiomers and/or diastereomers, in any mixing ratio, or a corresponding salt thereof, or a corresponding solvate thereof.

In a preferred embodiment of the compound according to the invention of general Formula (I) and in relation to R_(1′) of any of the embodiments of the present invention,

-   -   the alkyl, alkenyl or alkynyl in R_(1′), if substituted, is         substituted with one or more substituent/s selected from —OR₁₁,         halogen, —CN, haloalkyl, haloalkoxy and —NR₁₁R_(11′″);         optionally in form of one of the stereoisomers, preferably         enantiomers or diastereomers, a racemate or in form of a mixture         of at least two of the stereoisomers, preferably enantiomers         and/or diastereomers, in any mixing ratio, or a corresponding         salt thereof, or a corresponding solvate thereof.

In a preferred embodiment of the compound according to the invention of general Formula (I) and in relation to R₂ of any of the embodiments of the present invention,

-   -   the cycloalkyl, aryl or heterocyclyl in R₂, if substituted, is         substituted with one or more substituent/s selected from         halogen, —R₂, —OR₁₂, —NO₂, —NR₁₂R_(12′″), NR₁₂C(O)R_(2′),         —NR₁₂S(O)₂R_(12′), —S(O)₂NR₁₂R_(12′), —NR₁₂C(O)NR_(12′)R_(12″),         —SR₁₂, —S(O)R₁₂, S(O)₂R₁₂, —CN, haloalkyl, haloalkoxy,         —C(O)OR₁₂, —C(O)NR₁₂R_(12′), —OCH₂CH₂OH,         —NR₁₂S(O)₂NR_(12′)R_(12″) and C(CH₃)₂OR₁₂;         optionally in form of one of the stereoisomers, preferably         enantiomers or diastereomers, a racemate or in form of a mixture         of at least two of the stereoisomers, preferably enantiomers         and/or diastereomers, in any mixing ratio, or a corresponding         salt thereof, or a corresponding solvate thereof.

In a preferred embodiment of the compound according to the invention of general Formula (I) and in relation to R₂ of any of the embodiments of the present invention,

-   -   the cycloalkyl or non-aromatic heterocyclyl in R₂, if         substituted, may also be substituted with

or ═O;

optionally in form of one of the stereoisomers, preferably enantiomers or diastereomers, a racemate or in form of a mixture of at least two of the stereoisomers, preferably enantiomers and/or diastereomers, in any mixing ratio, or a corresponding salt thereof, or a corresponding solvate thereof.

In a preferred embodiment of the compound according to the invention of general Formula (I) and in relation to R₂ of any of the embodiments of the present invention,

-   -   the alkyl, alkenyl or alkynyl in R₂, if substituted, is         substituted with one or more substituent/s selected from —OR₁₂,         halogen, —CN, haloalkyl, haloalkoxy and —NR₁₂R_(12′″);         optionally in form of one of the stereoisomers, preferably         enantiomers or diastereomers, a racemate or in form of a mixture         of at least two of the stereoisomers, preferably enantiomers         and/or diastereomers, in any mixing ratio, or a corresponding         salt thereof, or a corresponding solvate thereof.

In a preferred embodiment of the compound according to the invention of general Formula (I) and in relation to alkyls other than those defined in R₁ or R₂ of any of the embodiments of the present invention,

the alkyl, alkenyl or alkynyl, other than those defined in R_(1′) or R₂, if substituted, is substituted with one or more substituent/s selected from —OR₁₃, halogen, —CN, haloalkyl, haloalkoxy and —NR₁₃R_(13′″); optionally in form of one of the stereoisomers, preferably enantiomers or diastereomers, a racemate or in form of a mixture of at least two of the stereoisomers, preferably enantiomers and/or diastereomers, in any mixing ratio, or a corresponding salt thereof, or a corresponding solvate thereof.

In a preferred embodiment of the compound according to the invention of general Formula (I) and in relation to the cycloalkyl, aryl or heterocyclyl other than those defined in R_(1′) or R₂ of any of the embodiments of the present invention,

the aryl, heterocyclyl or cycloalkyl other than those defined in R_(1′) or R₂, if substituted, is substituted with one or more substituent/s selected from halogen, —R₁₄, —OR₁₄, —NO₂, —NR₁₄R_(14′″), NR₁₄C(O)R_(14′), —NR₁₄S(O)₂R_(14′), —S(O)₂NR₁₄R_(14′), —NR₁₄C(O)NR_(14′)R_(14″), —SR₁₄, —S(O)R₁₄, S(O)₂R₁₄, —CN, haloalkyl, haloalkoxy, —C(O)OR₁₄, —C(O)NR₁₄R_(14′), —OCH₂CH₂OH, —NR₁₄S(O)₂NR_(14′)R_(14″) and C(CH₃)₂OR₁₄; optionally in form of one of the stereoisomers, preferably enantiomers or diastereomers, a racemate or in form of a mixture of at least two of the stereoisomers, preferably enantiomers and/or diastereomers, in any mixing ratio, or a corresponding salt thereof, or a corresponding solvate thereof.

In a preferred embodiment of the compound according to the invention of general Formula (I) and in relation to to the cycloalkyl, aryl or heterocyclyl other than those defined in R_(1′) or R₂ of any of the embodiments of the present invention,

the cycloalkyl or non-aromatic heterocyclyl, other than those defined in R_(1′) or R₂, if substituted, may also be substituted with

or ═O;

optionally in form of one of the stereoisomers, preferably enantiomers or diastereomers, a racemate or in form of a mixture of at least two of the stereoisomers, preferably enantiomers and/or diastereomers, in any mixing ratio, or a corresponding salt thereof, or a corresponding solvate thereof.

In an embodiment of the compound according to the invention of general Formula (I),

the halogen is fluorine, chlorine, iodine or bromine, preferably fluorine or chlorine; optionally in form of one of the stereoisomers, preferably enantiomers or diastereomers, a racemate or in form of a mixture of at least two of the stereoisomers, preferably enantiomers and/or diastereomers, in any mixing ratio, or a corresponding salt thereof, or a corresponding solvate thereof.

In an embodiment of the compound according to the invention of general Formula (I),

the haloalkyl is —CF₃; optionally in form of one of the stereoisomers, preferably enantiomers or diastereomers, a racemate or in form of a mixture of at least two of the stereoisomers, preferably enantiomers and/or diastereomers, in any mixing ratio, or a corresponding salt thereof, or a corresponding solvate thereof. In another embodiment of the compound according to the invention of general Formula (I), the haloalkoxy is —OCF₃; optionally in form of one of the stereoisomers, preferably enantiomers or diastereomers, a racemate or in form of a mixture of at least two of the stereoisomers, preferably enantiomers and/or diastereomers, in any mixing ratio, or a corresponding salt thereof, or a corresponding solvate thereof.

As this invention is aimed at providing a compound or a chemically related series of compounds which act as ligands of the σ₁ receptor it is a very preferred embodiment in which the compounds are selected which act as ligands of the σ₁, receptor and especially compounds which have a binding expressed as K_(i) which is preferably <1000 nM, more preferably <500 nM, even more preferably <100 nM.

In the following the phrase “compound of the invention” is used. This is to be understood as any compound according to the invention as described above according to general Formula (I), (I′), (I^(a′)), (I^(b′)), (I^(2′)), (I^(3′)) or (I^(4′)).

The compounds of the invention represented by the above described Formula (I) may include enantiomers depending on the presence of chiral centres or isomers depending on the presence of multiple bonds (e.g. Z, E). The single isomers, enantiomers or diastereoisomers and mixtures thereof fall within the scope of the present invention.

For the sake of clarity the expression “a compound according to Formula (I), wherein R₁, R₂, R₃, R_(3′), R₅, R_(5′), R₆, R_(6′), R_(n), X, Y, m and n are as defined in the description in the detailed description” would (just like the expression “a compound of Formula (I) as defined in any one of claims 1 to 10” found in the claims) refer to “a compound according to Formula (I)”, wherein the definitions of the respective substituents R₁ etc. (also from the cited claims) are applied. In addition, this would also mean, though (especially in regards to the claims) that also one or more disclaimers defined in the description (or used in any of the cited claims like e.g. claim 1) would be applicable to define the respective compound. Thus, a disclaimer found in e.g. claim 1 would be also used to define the compound “of Formula (I) as defined in any one of claims 1 to 10”.

In general the processes are described below in the experimental part. The starting materials are commercially available or can be prepared by conventional methods.

A preferred aspect of the invention is also a process for the production of a compound according to Formula (I).

A preferred aspect of the invention is a process for the production of a compound according to Formula (I),

and wherein R₁, R_(1′), R₂, R₃, R_(3′), R₄, R_(4′), R₅, R_(5′), R₆, R_(6′), m, n, p, X and Y are as defined in the description, following schemes 1 to 4.

In all processes and uses described underneath, the values of R₁, R_(1′), R₂, R₃, R_(3′), R₄, R_(4′), R₅, R_(5′), R₆, R_(6′), m, n, p, X and Y are as defined in the description (unless otherwise stated), LG represents a leaving group, such such as halogen, mesylate, tosylate or triflate, with the proviso that when Y═CO it can only be chloro or bromo, V represents an aldehyde or another leaving group (such as halogen, mesylate, tosylate or triflate) and P′ represents a suitable protecting group (preferably 4-methoxybenzyl or benzyl).

A preferred embodiment of the invention is a process for the production of a compound according to Formula (I), wherein when R₁ is —(CR₄R_(4′))_(p)R_(1′), said process comprises:

-   -   a) the intramolecular cyclization of a compound of formula VII

-   -   or     -   b) the reaction of a compound of formula XI

with a compound of formula XVI

-   -   or     -   c) the incorporation of the group         —N(R_(n))(CR₅R_(5′))_(m)X(CR₆R_(6′))_(n)R₂ by reaction of a         ketone of formula VIIIK

-   -   with an amine of formula XVII

A preferred embodiment of the invention is a process for the production of a compound according to Formula (t), wherein when R₁ is —(CR₄R_(4′))_(p)R_(1′), said process comprises:

-   -   the intramolecular cyclization of a compound of formula VII

A preferred embodiment of the invention is a process for the production of a compound according to Formula (I), wherein when R₁ is —(CR₄R_(4′))_(p)R_(1′), said process comprises: the reaction of a compound of formula XI

-   -   with a compound of formula XVI

A preferred embodiment of the invention is a process for the production of a compound according to Formula (I), wherein when R₁ is —(CR₄R_(4′))_(p)R_(1′), said process comprises: the incorporation of the group —N(R_(n))(CR₅R_(5′))_(m)X(CR₆R_(6′))_(n)R₂ by reaction of a ketone of formula VIIK

-   -   with an amine of formula XVII

A preferred embodiment of the invention is a process for the production of a compound according to Formula (I), wherein R₁ is —(CR₄R_(4′))_(p)R_(1′) and wherein Y represents CO and R₃ and R_(3′) are taken together with the connecting C-atom to form a cycloalkyl (compound Id), said process comprises:

-   -   a) a cyclopropanation reaction of compounds of formula XXII

-   -   -   or

    -   b) the treatment of a compound of formula Ic, wherein r is 1,         and R_(r) and R_(r′) are hydrogen:

with a strong base in an aprotic solvent, at a suitable temperature; or

-   -   c) the reaction of a compound of formula XXVI

-   -   with a compound of formula XVI

A preferred embodiment of the invention is a process for the production of a compound according to Formula (I), wherein R₁ is —(CR₄R_(4′))_(p)R_(1′), Y represents CO and R₃ and R_(3′) are taken together with the connection C-atom to form a cycloalkyl (compound Ib),

said process comprises the treatment of a compound of formula Ic,

with a strong base in an aprotic solvent, at a suitable temperature.

A preferred embodiment of the invention is a process for the production of a compound according to Formula (I), wherein Y is CH₂ and R₁ is —C(O)—R_(1′) (compound of formula Io), said process comprises:

reacting a compound of formula XXXIV

with an acylating agent of formula XXXVI

In another particular embodiment a compound of Formula II, IIP, III, IIIP, XIII, XIIIP, XII, IV, V, VP, VI, XIV, XIVP, X, XP, VII, VIIP, XV, XVP, XVK, XI, XIP, XIK, XVI, VIIIP, VIIIK, XVII, Ie, XXIP, XXIK, XXII, XVIIIP, XVIIIK, Ic, XIX, XIXP, XXP, XXK, XXIV, XXIVP, XXIVK, XXVI, XXVIP, XXVIK, XXIIIP, XXIIIK, Ig, XXVP, XXVK, Ih, XXVIIP, XXVIIK, XXVIIIa, XXIXP, XXIXK, XXVIIIb, XXXP, XXXK, XXVIIIc, XVIIIP, XVIIIK, XVII, Im, XXXIIIP, XXXIIIK, In, XXXVP, XXXVK, XXXII, XXXIIP, XXXIIK, XXXIV, XXXIVP, XXXVI, XXXVIIP, XXXVIIK, XXXP, XXXK, XXXIP, XXXIK or XVII

is used for the preparation of a compound of Formula (I).

The obtained reaction products may, if desired, be purified by conventional methods, such as crystallisation and chromatography. Where the above described processes for the preparation of compounds of the invention give rise to mixtures of stereoisomers, these isomers may be separated by conventional techniques such as preparative chromatography. If there are chiral centers the compounds may be prepared in racemic form, or individual enantiomers may be prepared either by enantiospecific synthesis or by resolution.

One preferred pharmaceutically acceptable form of a compound of the invention is the crystalline form, including such form in pharmaceutical composition. In the case of salts and also solvates of the compounds of the invention the additional ionic and solvent moieties must also be non-toxic. The compounds of the invention may present different polymorphic forms, it is intended that the invention encompasses all such forms.

Another aspect of the invention refers to a pharmaceutical composition which comprises a compound according to the invention as described above according to general formula I or a pharmaceutically acceptable salt or steroisomer thereof, and a pharmaceutically acceptable carrier, adjuvant or vehicle. The present invention thus provides pharmaceutical compositions comprising a compound of this invention, or a pharmaceutically acceptable salt or stereoisomers thereof together with a pharmaceutically acceptable carrier, adjuvant, or vehicle, for administration to a patient.

Examples of pharmaceutical compositions include any solid (tablets, pills, capsules, granules etc.) or liquid (solutions, suspensions, or emulsions) composition for oral, topical or parenteral administration.

In a preferred embodiment the pharmaceutical compositions are in oral form, either solid or liquid. Suitable dose forms for oral administration may be tablets, capsules, syrops or solutions and may contain conventional excipients known in the art such as binding agents, for example syrup, acacia, gelatin, sorbitol, tragacanth, or polyvinylpyrrolidone; fillers, for example lactose, sugar, maize starch, calcium phosphate, sorbitol or glycine; tabletting lubricants, for example magnesium stearate; disintegrants, for example starch, polyvinylpyrrolidone, sodium starch glycollate or microcrystalline cellulose; or pharmaceutically acceptable wetting agents such as sodium lauryl sulfate.

The solid oral compositions may be prepared by conventional methods of blending, filling or tabletting. Repeated blending operations may be used to distribute the active agent throughout those compositions employing large quantities of fillers. Such operations are conventional in the art. The tablets may for example be prepared by wet or dry granulation and optionally coated according to methods well known in normal pharmaceutical practice, in particular with an enteric coating.

The pharmaceutical compositions may also be adapted for parenteral administration, such as sterile solutions, suspensions or lyophilized products in the appropriate unit dosage form. Adequate excipients can be used, such as bulking agents, buffering agents or surfactants.

The mentioned formulations will be prepared using standard methods such as those described or referred to in the Spanish and US Pharmacopoeias and similar reference texts.

Administration of the compounds or compositions of the present invention may be by any suitable method, such as intravenous infusion, oral preparations, and intraperitoneal and intravenous administration. Oral administration is preferred because of the convenience for the patient and the chronic character of the diseases to be treated.

Generally an effective administered amount of a compound of the invention will depend on the relative efficacy of the compound chosen, the severity of the disorder being treated and the weight of the sufferer. However, active compounds will typically be administered once or more times a day for example 1, 2, 3 or 4 times daily, with typical total daily doses in the range of from 0.1 to 1000 mg/kg/day.

The compounds and compositions of this invention may be used with other drugs to provide a combination therapy. The other drugs may form part of the same composition, or be provided as a separate composition for administration at the same time or at different time.

Another aspect of the invention refers to the use of a compound of the invention or a pharmaceutically acceptable salt or isomer thereof in the manufacture of a medicament.

Another aspect of the invention refers to a compound of the invention according as described above according to general formula I, or a pharmaceutically acceptable salt or isomer thereof, for use as a medicament for the treatment of pain. Preferably the pain is medium to severe pain, visceral pain, chronic pain, cancer pain, migraine, inflammatory pain, acute pain or neuropathic pain, allodynia or hyperalgesia. This may include mechanical allodynia or thermal hyperalgesia.

Another aspect of the invention refers to the use of a compound of the invention in the manufacture of a medicament for the treatment or prophylaxis of pain.

In a preferred embodiment the pain is selected from medium to severe pain, visceral pain, chronic pain, cancer pain, migraine, inflammatory pain, acute pain or neuropathic pain, allodynia or hyperalgesia, also preferably including mechanical allodynia or thermal hyperalgesia.

Another aspect of this invention relates to a method of treating or preventing pain which method comprises administering to a patient in need of such a treatment a therapeutically effective amount of a compound as above defined or a pharmaceutical composition thereof. Among the pain syndromes that can be treated are medium to severe pain, visceral pain, chronic pain, cancer pain, migraine, inflammatory pain, acute pain or neuropathic pain, allodynia or hyperalgesia, whereas this could also include mechanical allodynia or thermal hyperalgesia.

The present invention is illustrated below with the aid of examples. These illustrations are given solely by way of example and do not limit the general spirit of the present invention.

General Experimental Part (Methods and Equipment of the Synthesis and Analysis Scheme 1:

A 4-step process is described for the preparation of compounds of general formula (I) wherein R₁ is —(CR₄R_(4′))_(p)R_(1′) (compounds of formula Ia) starting from a ketone of formula II, as shown in the following scheme:

wherein R_(1′), R₂, R₃, R_(3′), R₄, R_(4′), R₅, R_(5′), R₆, R_(6′), R_(n), X, Y, m, n and p have the meanings as defined above for a compound of formula (I), LG represents a leaving group, such such as halogen, mesylate, tosylate or triflate, with the proviso that when Y═CO it can only be chloro or bromo, V represents an aldehyde or another leaving group (such as halogen, mesylate, tosylate or triflate) and P′ represents a suitable protecting group (preferably 4-methoxybenzyl or benzyl).

The 4 step-process is carried out as described below:

Step 1: A compound of formula III is prepared by treating a compound of formula II with a suitable methyl-transfer reagent such as trimethylsulfoxonium iodide or trimethylsulfonium iodide, in a suitable aprotic solvent such as dimethylsulfoxide or 1,2-dimethoxyethane or mixtures, and in the presence of a strong base such as sodium hydride or potassium tert-butoxide, at a suitable temperature, preferably comprised between 0° C. and 60° C. Step 2: A compound of formula V is prepared by reacting a compound of formula III with an amine of formula IV, in a suitable solvent such as an alcohol, preferably ethanol-water mixtures, at a suitable temperature comprised between room temperature and the reflux temperature. Step 3: A compound of formula VII is prepared by reacting a compound of formula V with a compound, of formula VI. Depending on the meaning of Y, the compound of formula VI can be of different nature and different reaction conditions will apply:

-   -   a) When Y represents CO, VI is an acylating agent. The acylation         reaction is carried out in a suitable solvent, such as         dichloromethane or ethyl acetate-water mixtures; in the presence         of an organic base such as triethylamine or         diisopropylethylamine or an inorganic base such as K₂CO₃; and at         a suitable temperature, preferably comprised between −78° C. and         room temperature.     -   b) When Y represents CH₂, VI is an alkylating agent. The         alkylation reaction may be carried out in a suitable solvent,         such as acetonitrile, dichloromethane, tetrahydrofuran,         1,4-dioxane or dimethylformamide; in the presence of an         inorganic base such as K₂CO, Cs₂CO₃ or NaH, or an organic base         such as triethylamine or diisopropylethylamine, at a suitable         temperature comprised between room temperature and the reflux         temperature. The OH group present may need protection previous         to the alkylation reaction.         Step 4: The intramolecular cyclization of a compound of formula         VII renders a compound of formula Ia. The cyclization reaction         is carried out in a suitable solvent, such as tetrahydrofuran;         in the presence of a strong base such as potassium tert-butoxide         or sodium hydride; and at a suitable temperature, comprised         between −78° C. and the reflux temperature, preferably cooling.

Alternatively, the group —N(R_(n))(CR₅R_(5′))_(m)X(CR₆R_(6′))_(n)R₂ can be incorporated in the last step of the synthesis by reaction of a ketone of formula VIIIK with an amine of formula XVII to render a compound of formula Ia, as shown in Scheme 1. A compound of formula VIIIK is obtained by hydrolysis of a compound of formula VIIIP, wherein A and A′ together with the C atom where they are attached represent a suitable ketal group (cyclic or acyclic). The deprotection can be conducted by adding a solution of an acid such as HCl, in a suitable solvent such as tetrahydrofuran or water or mixtures, at a suitable temperature comprised between room temperature and the reflux temperature, preferably heating. A compound of formula VIIIP is prepared from a compound of formula IIP following the same sequence described for the synthesis of compounds of formula Ia.

The reductive amination reaction between a compound of formula VIIIK and a compound of formula XVII is carried out in the presence of a reductive reagent, preferably sodium triacetoxyborohydride, in an aprotic solvent, preferably tetrahydrofuran, dichloromethane or dichloroethane, optionally in the presence of an acid, preferably acetic acid.

In another alternative approach, the —(CR₄R_(4′))_(p)R_(1′) substituent can be incorporated later in the sequence by the reaction of a compound of formula XI with a compound of formula XVI. Depending on the meaning of Y, V can be of different nature and different reaction conditions will apply:

-   -   a) When Y is CH₂, compound XVI is an alkylating agent and V         represents a leaving group such as halogen, mesylate, tosylate         or triflate. The alkylation reaction is carried out in a         suitable solvent, such as acetonitrile, dichloromethane,         1,4-dioxane or dimethylformamide; in the presence of an         inorganic base such as K₂CO₃, Cs₂CO₃ or sodium hydride, or an         organic base such as triethylamine or diisopropylethylamine, at         a suitable temperature comprised between room temperature and         the reflux temperature. Additionally, an, activating agent such         as NaI can be used.         -   Alternatively, compound XVI can be an aldehyde wherein V             represents a C(O)—H group. The reductive amination reaction             between a compound of formula XVI and a compound of formula             XI is carried out under the same reaction conditions             described above for the reaction of a compound of formula             VIIIK and a compound of formula XVII.     -   b) When Y is C(O), compound XVI is an alkylating agent and V         represents a leaving group such as halogen, mesylate, tosylate         or triflate. This alkylation reaction is carried out in an         aprotic solvent, preferably dimethylformamide or         tetrahydrofuran, in the presence of an inorganic base such as         NaH, at a suitable temperature, preferably between room         temperature and 60° C.

A compound of formula XI is synthesized following an analogous sequence as described for the synthesis of compounds of formula Ia, but effecting step 2 using ammonia instead of an amine IV. Alternatively, when Y is C(O), a compound of formula XI can be prepared by reaction of a compound of formula XIK (prepared from a compound of formula XIP, wherein A and A′ together with the C atom where they are attached represent a suitable ketal group) with a compound of formula XVII, as described above.

Additionally, a compound of formula XI can be prepared from a compound of formula XV, wherein P′ represents a suitable protecting group. When Y is C(O), P′ is preferably a 4-methoxybenzyl group and the deprotection reaction is carried out with cerium ammonium nitrate in a suitable solvent such as mixtures of acetonitrile-water or by heating in trifluoroacetic acid or hydrochloric acid. When Y is —CH₂—, P is preferably a 4-methoxybenzyl or a benzyl group, and the deprotection reaction is preferably carried out by hydrogenation under hydrogen atmosphere and metal catalysis, preferably by the use of palladium over charcoal as catalyst in a suitable solvent such as methanol or ethanol, optionally in the presence of an acid such as acetic acid or hydrochloric acid.

A compound of formula XV is synthesized from a compound of formula III and an amine of formula XII following an analogous sequence as described for the synthesis of compounds of formula Ia. Alternatively, a compound of formula XV can be prepared by reaction of a compound of formula XVK (prepared from a compound of formula XVP, wherein A and A′ together with the C atom where they are attached represent a suitable ketal group) with a compound of formula XVII, as described above.

The compounds of general formula II, IIP, IV, VI, XII, XVI and XVII are commercially available or can be prepared by conventional methods described in the bibliography.

Scheme 2

The preparation of compounds of general formula (I) wherein Y represents CO and R₃ and R_(3′) are taken together with the connecting C-atom to form a cycloalkyl (compounds of formula Ib) is described in the following scheme:

Wherein R_(1′), R₂, R₄, R_(4′), R₅, R_(5′), R₆, R_(6′), R_(n), X, m, n and p have the meanings as defined above for a compound of formula (I), r represents 1, 2, 3 or 4, R_(r) and R_(r′) represent hydrogen or any substitution according to the present invention, LG represents a leaving group such as halogen, mesylate, tosylate or triflate, V represents another leaving group (such as halogen, mesylate, tosylate or triflate), P′ represents a suitable protecting group (preferably 4-methoxybenzyl) and Q represents methyl or benzyl.

A compound of formula Ib can be prepared from a compound of formula Ic by treatment with a strong base such as lithium diisopropylamide or potassium tert-butoxide, in an aprotic solvent such as tetrahydrofuran, at a suitable temperature, preferably cooling. And analogously, a compound of formula Id (wherein R_(r)═R_(r′)═H and r=1) can be prepared from a compound of formula Ic under the same reaction conditions.

Alternatively, compounds of formula Id can be prepared from compounds of formula XXII. The cyclopropanation reaction is carried out using a suitable methyl-transfer reagent such as trimethylsulfoxonium iodide or trimethylsulfonium iodide, in a suitable aprotic solvent such as dimethylsulfoxide, and in the presence of a strong base such as sodium hydride or potassium tert-butoxide, at a suitable temperature, preferably comprised between room temperature and 60° C. Alternatively, typical Simmons-Smith reaction conditions could be used, comprising the treatment of a compound of formula XXII with diiodomethane, a zinc source such as zinc-copper, zinc iodide or diethylzinc, in a suitable aprotic solvent, such as diethyl ether.

Compounds of formula XXII can be prepared from a compound of formula Ie wherein Q represents methyl or benzyl. The elimination reaction is carried out in the presence of a base, such as potassium tert-butoxide, in a suitable solvent, such as tetrahydrofuran.

In another alternative approach, the —(CR₄R_(4′))_(p)R_(1′) substituent can be incorporated later in the synthesis. Thus, compounds of formula Ib and Id can be prepared from compounds of formula XXIV and XXVI, respectively, following the reaction conditions described in Scheme 1 for the preparation of compounds of formula Ia from compounds of formula XI. The compounds of formula XXIV and XXVI can be prepared from suitable protected precursors If and Ig, respectively, following the conditions described in Scheme 1.

The protected compounds of general formula If and Ig can be prepared following an analogous procedure to the one described in Scheme 2 for the preparation of compounds Ib and Id from compounds of formula Ic, using suitable precursors.

In addition, the group —N(R_(n))(CR₅R_(5′))_(m)X(CR₆R_(6′))_(m)R₂ can be incorporated in the last step of the synthesis to prepare compounds of formula Ib, Id, Ie, If, Ig, XXIV and XXVI from suitable protected precursors, by deprotection followed by reaction with a compound of formula XVII, as described in Scheme 1 for the preparation, of compounds of formula Ia.

The compounds of general formula Ic and Ie can be prepared by the procedures described in Scheme 1 from a compound of formula V using suitable starting materials.

Scheme 3 and Scheme 4

Compounds of formula (I) can also be prepared starting from other compounds of formula (I), as described in Schemes 3 and 4 below.

Compounds of formula Ib, Ii and Ij can be prepared from a compound of formula Ih as shown in Scheme 3:

wherein R_(1′), R₂, R₃, R_(3′), R₄, R_(4′), R₅, R_(5′), R₆, R_(6′), R_(n), X, m, n and p have the meanings as defined above for a compound of formula (I), r represents 1, 2, 3 or 4, R_(r) and R_(r′) represent hydrogen or any substitution according to the present invention, and X′ and X″ independently represent a leaving group such as halogen, mesylate, tosylate or triflate.

A compound of formula Ii can be prepared by treating a compound of formula Ih with an alkylating agent of formula XXVIIIa in the presence of a strong base such as lithium diisopropylamide or potassium tert-butoxide, in an aprotic solvent such as tetrahydrofuran, at a suitable temperature, preferably comprised between −78° C. and room temperature. A second alkylation can be performed under the same reaction conditions to prepare a compound of formula Ij. An analogous double-alkylation process can be used for the preparation of compounds of formula Ib, by reacting a compound of formula Ih with an alkylating agent of formula XXVIIIc, as an alternative to the procedure described in Scheme 2 for the preparation of compounds of formula Ib.

In addition, the group —N(R_(n))(CR₅R_(5′))_(m)X(CR₆R_(6′))_(n)R₂ can be incorporated in the last step of the synthesis to prepare compounds of formula Ib, Ih, Ii and Ij from suitable protected precursors, by deprotection followed by reaction with a compound of formula XVII, under the reaction conditions described in Scheme 1 for the preparation of compounds of formula Ia.

The compounds of general formula Ih and Ii can be prepared by the procedures described in Scheme 1 using suitable starting materials.

Scheme 4 shows the preparation of compounds of formula (I) wherein Y is CH₂ from compounds of formula (I) wherein Y is C(O):

wherein R_(1′), R₂, R₃, R_(3′), R₄, R_(4′), R₅, R_(5′), R₆, R_(6′), R_(n), X, m, n and p have the meanings as defined above for a compound of formula (I), V represents an aldehyde or a leaving group (such as halogen, mesylate, tosylate or triflate), P′ represents a suitable protecting group (preferably 4-methoxybenzyl or benzyl) and Z represents OH or halogen (preferably bromo or chloro).

The reduction reaction of a compound of formula Ij or to Io yield a compound of formula Ik can be performed using a suitable reducing agent such as lithium aluminium hydride, borane-tetrahydrofuran complex or borane-dimethyl sulphide complex, in a suitable solvent such as tetrahydrofuran or diethyl ether, at a suitable temperature comprised between room temperature and the reflux temperature, preferably heating.

The reduction reaction can also be performed on a suitable precursor (compounds of formula Im or XXXII) or a protected derivative (compounds of formula XXXIIIP, XXXIIP or XXXVIIP).

The compounds of general formula Ij can be prepared by the procedures described in Schemes 1 to 3 using suitable starting materials, or they can be prepared from a compound of formula Im or XXXII. The deprotection of a compound of formula Im to give a compound of formula XXXII and the subsequent reaction with a compound of formula XVI to yield a compound of formula Ij are performed following the procedures described in Scheme 1.

The compounds of general formula Im and XXXII can be prepared according to the procedures described in Scheme 1 using suitable starting materials.

Accordingly, the compounds of general formula Ik may be prepared from a compound of formula In or XXXIV following an analogous procedure.

A compound of formula Io is prepared by reacting a compound of formula XXXIV with an acylating agent of formula XXXVI. When Z is halogen, the reaction is carried out in a suitable solvent, such as dichloromethane, tetrahydrofuran, ethyl acetate or ethyl acetate-water mixtures; in the presence of an organic base such as triethylamine or diisopropylethylamine or an inorganic base such as K₂CO₃; and at a suitable temperature, preferably comprised between 0° C. and room temperature. Additionally, an activating agent such as 4-dimethylaminopyridine can be used.

When Z is OH, the acylation reaction is carried out using a suitable coupling reagent such as N-(3-dimethylaminopropyl)-N′-ethylcarbodiimide (EDC), dicyclohexylcarbodiimide (DCC), N-[(dimethylamino)-1H-1,2,3-triazolo-[4,5-b]pyridin-1-ylmethylene]-N-methmetylmethanaminium hexafluorophosphate N-oxide (HATU) or N,N,N′,N′-tetramethyl-O-(1H-benzotriazol-1-yl)uronium hexafluorophosposphate (HBTU), optionally in the presence of 1-hydroxybenzotriazole, optionally in the presence of an organic base such as N-methylmorpholine or diisopropylethylamine, in a suitable solvent such as dichloromethane or dimethylformamide, and at a suitable temperature, preferably at room temperature.

In addition, the group —N(R_(n))(CR₅R_(5′))_(m)X(CR₆R_(6′))_(n)R₂ may be incorporated at different stages of the synthesis to prepare compounds of formula Ik and to from suitable precursors and a compound of formula XVII, following similar reaction conditions as described in Scheme 1 for the preparation of compounds of formula Ia.

Moreover, certain compounds of the present invention can also be obtained starting from other compounds of formula (I) by appropriate conversion reactions of functional groups, in one or several steps, using well-known reactions in organic chemistry under standard experimental conditions. As a way of example, some of these conversions include the N-debenzylation of an amine to yield a NH group, and the alkylation or reductive amination of a secondary amine to yield a tertiary amine.

In addition, a compound of formula I that shows chirality can also be obtained by resolution of a racemic compound of formula I either by chiral preparative HPLC or by crystallization of a diastereomeric salt or co-crystal. Alternatively, the resolution step can be carried out at a previous stage, using any suitable intermediate.

EXAMPLES Intermediates and Examples

The following abbreviations are used in the examples:

ACN: acetonitrile AcOH: acetic acid DCM: dichloromethane DME: 1,2-dimethoxyetane DMSO: dimethyl sulfoxide

EtOH: Ethanol

EX: example h: hour/s HPLC: high performance liquid chromatography INT: intermediate LDA: lithium diisopropylamide MeOH: methanol MS: mass spectrometry Min.: minutes Quant: quantitative Ret.: retention r.t.: room temperature Sat: saturated s.m.: starting material TFA: trifluoroacetic acid THF: tetrahydrofuran Wt: weight

The following method was used to determine the HPLC-MS spectra:

Column: Gemini-NX 30×4.6 mm, 3 um Temperature: 400

Flow: 2.0 mL/min Gradient: NH₄HCO₃ pH 8: ACN (95:5)-0.5 min(95:5)-6.5 min-(0:100)-1 min-(0:100) Sample dissolved approx. 1 mg/mL in NH₄HCO₃ pH 8/ACN

Alternatively, method B was used in some cases and is indicated in examples and tables as (B):

Method B Column: Kinetex EVO 50×4.6 mm 2.6 um Temperature: 40° C.

Flow: 2.0 mL/min Gradient: NH₄HCO₃ pH 8: ACN (95:5)-0.5 min-(95:5)-6.5 min-(0:100)-1 min-(0:100) Sample dissolved approx. 1 mg-mL in NH₄HCO₃ pH 8/ACN

Synthesis of Intermediates Intermediate 1: 1,7,10-Trioxadispiro[2.2.4.2]dodecane

To a solution of potassium tert-butoxide (14.5 g, 130 mmol) in DMSO (83 mL), trimethylsulfoxonium iodide (31.8 g, 144 mmol) was added in portions. The mixture was stirred at r.t. for 1.5 h. DME (23 mL) was added and it was cooled to 0-5° C. A solution of 1,4-dioxaspiro[4.5]decan-8-one (15.56 g, 99.6 mmol) in a mixture of DME (23 mL) and DMSO (7.5 mL) was added dropwise. The reaction mixture was stirred at 0-5° C. for 1 h. It was diluted with water and ethyl acetate. The phases were separated and the aqueous phase was back extracted with additional ethyl acetate. The organic phases were combined, washed with water, dried over MgSO₄ and concentrated under vacuum to give the title compound (12.3 g, 72% yield).

Intermediate 2A: 8-((Ethylamino)methyl)-1,4-dioxaspiro[4.5]decan-8-ol

To a solution of intermediate 1 (5.0 g, 29.4 mmol) in a mixture of ethanol-water 9:1 (50 mL), ethylamine (46.7 mL, 70% solution in water, 587 mmol) was added. The reaction mixture was stirred at r.t. overnight. The solvent was removed under vacuum to give the title compound (6.3 g, quant, yield).

Intermediate 2B: 8-((Phenylamino)methyl)-1,4-dioxaspiro[4.5]decan-8-ol

To a solution of intermediate 1 (7.09 g, 41.7 mmol) in a mixture of ethanol-water 9:1 (140 mL), aniline (3.8 mL, 41.7 mmol) was added. The reaction mixture was heated to 100° C. overnight in an autoclave reactor. The solvent was removed under vacuum and the residue was purified by flash chromatography, silica gel, gradient dichloromethane to methanol:dichloromethane (1:4) to give the title compound (6.37 g, 58% yield).

Intermediate 2C: 8-(((4-M ethoxybenzyl)amino)methyl)-1,4-dioxaspiro[4,5]decan-8-ol

To a solution of intermediate 1 (14.9 g, 87.5 mmol) in a mixture of EtOH—H₂O 9:1 (75 mL), 4-methoxybenzylamine (11.4 mL, 87.5 mmol) was added. The reaction mixture was stirred at r.t. overnight. The solvent was removed under vacuum to give the title compound (29.3 g. overweight, quant. yield assumed).

Intermediate 3A: 16-Ethyl-4,9,12-trioxa-16-azatrispiro[2.1.2.4.2.3]heptadecan-17-one

Step 1. 2-Bromo-4-chloro-N-ethyl-((8-hydroxy-1,4-dioxaspiro[4.5]decan-8-yl)methyl)butanamide: To a solution of intermediate 2A (6.32 g, 29.4 mmol) in ethyl acetate (63 mL), a solution of K₂CO₃ (11.4 g, 82.2 mmol) in water (43 mL) was added. After cooling to 0-5° C., a solution of 2-bromo-4-chlorobutanoyl chloride (prepared as described in U.S. Pat. No. 6,114,541A1 (2000) Ex1) (8.78 g, 39.9 mmol) in ethyl acetate (15 mL) was added dropwise. The reaction mixture was stirred at 0-5° C. for 1 h and then it was diluted with water. The layers were separated and the aqueous phase was extracted with ethyl acetate. The organic phases were combined, washed with 0.5 M HCl aqueous solution and then NaHCO₃ sat solution, dried over MgSO₄, filtered and concentrated to dryness to give the title compound (9.86 g, crude product, 84% yield).

Step 2. Title compound: A solution of the crude product obtained in step 1 (8.86 g, 22.2 mmol) in THF (89 mL) was cooled under nitrogen to −78° C. After addition of potassium tert-butoxide solution (44.5 mL, 1M in THF, 44.5 mmol), the reaction mixture was stirred at −30° C. for 2 h. It was then warmed-up to 0-5° C. and additional potassium tert-butoxide solution (44.5 mL, 1M in THF, 44.5 mmol) was added. The mixture was stirred at 0-5° C. for 2 h. NH₄Cl sat solution was then added, it was further diluted with water and the aqueous phase was extracted 3 times with ethyl acetate. The organic phases were combined, dried over MgSO₄, filtered and concentrated under vacuum to give the title compound (5.49 g, 88% yield).

This method was used for the preparation of intermediates 3B-3C using suitable starting materials:

INT Structure Chemical name s.m. 3B

16-phenyl-4,9,12- trioxa-16- azatrispiro[2.1,2,4.2.3] heptedecan-17-one 2B 3C

16-(4-methoxybenzyl)- 4,9,12-trioxa-16- azatrispiro[2.1.2.4.2.3] heptadecen-17-one 2C

Intermediate 3D: 12-Ethyl-1,4,9-trioxa-12-azadispiro[4.2.5.2]pentadecan-11-one

Step 1. 2-Chloro-N-ethyl-N-((8-hydroxy-1,4-dioxaspiro[4.5]decan-8-yl)methyl)acetamide: To a solution of intermediate 2A (6 g, 27.9 mmol) in ethyl acetate (60 mL), a solution of K₂CO₃ (10.8 g, 78.0 mmol) in water (42 mL) was added. After cooling to 0° C., a solution 2-chloroacetyl chloride (4.28 g, 37.9 mmol) in ethyl acetate (15 mL) was added dropwise. The reaction mixture was stirred at 0-5° C. for 1 h and then it was diluted with water. The layers were separated and the aqueous phase was extracted with ethyl acetate. The organic phases were combined, washed with 0.5 M HCl aqueous solution and then NaHCO₃ sat solution, dried over MgSO₄, filtered and concentrated to dryness to give the title compound (4.94 g, 61% yield).

Step 2. Title compound: A solution of the crude product obtained in Step 1 (4.93 g, 16.9 mmol) in THF (50 mL) was cooled to −78° C. using a dry ice/acetone bath. After addition of potassium tert-butoxide solution (25.4 mL, 1M in THF, 25.4 mmol), the reaction mixture was stirred at −78° C. for 1 h. NH₄Cl sat solution was then added, and the aqueous phase was extracted with ethyl acetate (×3). The organic phases were combined, dried over MgSO₄, filtered and concentrated under vacuum to give the title compound (3.77 g, 87% yield).

Intermediate 3E: 12-Ethyl-10,10-dimethyl-1,4,9-trioxa-12-azadispiro[4.2.5.2]pentadecan-11-one

Step 1. 12-Ethyl-10-methyl-1,4,9-trioxa-12-azadispiro[4.2.5.2]pentadecan-11-one. The product was prepared following the procedure described for the preparation of Intermediate 3D, starting from intermediate 2A and 2-chloropropanoyl chloride.

Step 2. Title compound: A solution of the product obtained in Step 1 (7.5 g, 27.8 mmol) in dry THF (39 mL) was cooled to 0-5° C. under a nitrogen atmosphere. After slow addition of LDA solution (37.2 mL, 1.5 M in THF/n-heptane/ethylbenzene, 55.8 mmol), the reaction mixture was stirred at 0-5° C. for 30 min. Iodomethane (5.2 mL, 83.5 mmol) was then added and the reaction mixture was stirred at 0-5° C. for further 60 min. A second round of LDA solution and iodomethane were added to get the reaction to completion. NH₄Cl sat solution was then added, and the aqueous phase was extracted three times with ethyl acetate. The combined organic phases were dried over Na₂SO₄, filtered and concentrated under vacuum. The residue was purified by flash chromatography, silica gel, gradient dichloromethane to methanol:dichloromethane (1:8) to give the title compound (5.02 g, 62% yield).

Intermediate 4A: 12-Ethyl-4-oxa-12-azadispiro[2.1.5.3]tridecane-8,13-dione

To a solution of intermediate 3A (6.1 g, 21.7 mmol) in THF (116 mL), 6 M HCl aqueous solution (36 mL, 217 mmol) was added. The reaction mixture was heated to 50° C. for 2 days in a sealed vessel. The volatiles were removed under vacuum and pH was adjusted to 7 with addition of NaHCO₃ sat solution. The aqueous phase was extracted 3 times with ethyl acetate. The organic phases were combined, washed with brine, dried over MgSO₄, filtered and concentrated under vacuum to give the title compound (5.15 g, crude product, quant. yield).

This method was used for the preparation of intermediate 4B using suitable starting materials:

INT Structure Chemical name s.m. 4B

12-phenyl-4-oxa-12- azadispiro[2.1.5.3]- tridecane-8,13-dione 3B

Intermediate 4C: 4-Ethyl-1-oxa-4-azaspiro[5.5]undecane3,9-dione

A solution of intermediate 3D (1.11 g, 4.35 mmol) in TFA (16.8 mL) was heated to 80° C. for 2 days in a sealed vessel. The volatiles were removed under vacuum to give the title compound as a crude product (1.81 g, overweight, quant, yield assumed).

This method was used for the preparation of intermediates 4D-E using suitable starting materials:

INT Structure Chemical name s.m. 4D

4-ethyl-2,2- dimethyl-1-oxa-4- azaspiro[5.5] undecane-3,9- dione 3E 4E

4-oxa-12- azadispiro[2.1.5.3] tridecane-8,13-dione 3C

Intermediates 5A and 5B: (5s,8s)-8-(Benzylamino)-4-oxa-12-azadispiro[2.1.5.3]tridecan-13-one and (5r,8r)-8-(benzylamino)-4-oxa-12-azadispiro[2.1.5.3]tridecan-13-one

To a solution of intermediate 4E (2.8 g, 13.4 mmol) in dry THF (138 mL), benzylamine (1.46 mL, 13.4 mmol) and sodium triacetoxyborohydride (3.77 g, 17.8 mmol) were added. The resulting mixture was stirred at r.t. overnight. 1N NaOH was added and it was extracted with DCM. The organic phases were combined, dried over Na₂SO₄, filtered and concentrated to dryness. The residue was purified by flash chromatography, C₁₆, gradient aqueous NH₄HCO₃ pH 8 to acetonitrile, to give intermediates 5A (856 mg, 21% yield) and 5B (209 mg, 5% yield).

Synthesis of Examples Examples 1 and 2: (5s,8s)-8-(Benzylamino)-12-ethyl-4-oxa-12-azadispiro[2.1.5.3]tridecan-13-one and (5r,8r)-8-(benzylamino)-12-ethyl-4-oxa-12-azadispiro[2.1.5.3]tridecan-13-one

To a solution of intermediate 4A (90 mg, 0.38 mmol) in dry THF (3.8 mL), benzylamine (0.041 mL, 0.38 mmol), acetic acid (0.022 mL, 0.38 mmol) and sodium triacetoxyborohydride (107 mg, 0.50 mmol) were sequentially added. The resulting mixture was stirred at r.t. for 4 h. 1N NaOH was added and it was extracted with DCM. The organic phases were combined, dried over Na₂SO₄, filtered and concentrated to dryness. The residue was purified by flash chromatography, C₁₈, gradient aqueous NH₄HCO₃ pH 8 to acetonitrile, obtaining examples 1 (25 mg, 20% yield) and 2 (27 mg, 22% yield)

HPLC retention time (Ex 1): 3.08 min; MS: 329.2 (M+H).

HPLC retention time (Ex 2): 3.36 min; MS: 329.2 (M+H).

This method was used for the preparation of examples 3-13 using suitable starting materials:

Ret time MS EX Structure Chemical name (min) (M + H) 3

(5s,8s)-12-ethyl-8- [methyl(2- phenylethyl)amino]-4- oxa-12- azadispiro[2.1.5.3] tridecan-13-one 3.61 357.2 4

(5r,8r)-12-ethyl-8- [methyl(2- phenylethyl)amino]-4- oxa-12- azadispiro[2.1.5.3] tridecan-13-one 3.90 357.2 5

(5s,8s)-8- [benzyl(methyl)amino]- 12-ethyl-4-oxo-12- azadispiro[2.1.5.3] tridecan-13-one 3.82 343.2 6

(5s,8s)-12-ethyl-8-[(2- phenylethyl)amino]-4- oxa-12- azadispiro[2.1.5.3] tridecan-13-one 3.16 343.2 7

(5r,8r)-12-ethyl-8-[(2- phenylethyl)amino]-4- oxa-12- azadispiro[2.1.5.3] tridecan-13-one 3.39 343.2 8

(5s,8s)-8- [benzyl(methyl)amino]- 12-phenyl-4-oxa-12- azadispiro[2.1.5.3] tridecan-13-one 4.59 391.2 9

(5s,8s)-8-[methyl(2- phenylethyl)amino]- 12-phenyl-4-oxa-12- azadispiro[2.1.5.3] tridecan-13-one 4.40 405.2 10

(5s,8s)-8- (benzylamino)-12- phenyl-4-oxa-12- azadispiro[2.1.5.3] tridecan-13-one 3.87 377.2 11

(5s,8s)-12-phenyl-8- [(2- phenylethyl)amino]-4- oxa-12- azadispiro[2.1.5.3] tridecan-13-one 3.90 391.2 12

(5r,8r)-8- (benzylamino)-12- phenyl-4-oxa-12- azadispiro[2.1.5.3] tridecan-13-one 4.08 377.2 13

(5r,8r)-12-phenyl- 8-[(2- phenytethyl)amino]-4- oxa-12- azadispiro[2.1.5.3] tridecan-13-one 4.05 391.2

Example 14: (5r,8r)-8-[Benzyl(methyl)amino]-12-phenyl-4-oxa-12-azadispiro[2.1.5.3]tridecan-13-one

To a solution of example 12 (37 mg, 0.098 mmol) in MeOH (0.4 mL), aqueous formaldehyde (0.13 mL, 37% Wt, 1.77 mmol) was added. The reaction mixture was stirred at r.t. for 30 min, and then sodium triacetoxyborohydride (62 mg, 0,295 mmol) was added in portions. The resulting mixture was stirred at r.t. for 5 h. NaHCO₃ sat solution was added and it was extracted with DCM. The organic phases were combined, dried over Na₂SO₄, filtered and concentrated to dryness. The residue was purified by flash chromatography, C₁₈, gradient aqueous NH₄HCO₃ pH 8 to acetonitrile, to give the title compound (15 mg, 39% yield).

HPLC retention time: 4.76 min; MS: 3912 (M+H).

This method was used for the preparation of examples 15-16 using suitable starting materials:

Ret time MS EX Structure Chemical name (min) (M + H) 15

(5r,8r)-8- [methyl(2- phenylethyl)amino]- 12-phenyl-4-oxa-12- azadispiro[2.1.5.3] tridecan-13-one 4.59 405.2 16

(5r,8r)-8- [benzyl(methyl)amino]- 12-ethyl-4-oxa- 12- azadispiro[2.1.5.3] tridecan-13-one 4.30 (B) 343.2

Example 17: (5s,8s)-N-Benzyl-12-ethyl-N-methyl-4-oxa-12-azadispiro[2.1.5.3]tridecan-8-amine

To a solution of example 5 (0.105 g, 0.30 mmol) in THF (0.2 mL), cooled at 0° C., LiAlH₄ solution (0.41 mL, 1M in THF, 0.41 mmol) was added dropwise. The reaction mixture was stirred at r.t. for 2 h. Then, NaHCO₃ sat solution was added and it was extracted with ethyl acetate. The organic phases were combined, washed with water, dried over Na₂SO₄, filtered and concentrated to dryness. The residue was purified by eluting through an acidic ion exchange resin cartridge (SCX), to give the title compound (73 mg, 73% yield).

HPLC retention time: 4.28 min; MS: 329.2 (M+H).

This method was used for the preparation of examples 18-20 using suitable starting materials:

Ret time MS EX Structure Chemical name (min) (M + H) 18

(5r,8r)-N-benzyl-12- ethyl-N-methyl-4- oxa-12- azadispiro[2.1.5.3] tridecan-8-amine 4.50 329.2 19

(5s,8s)-N-benzyl- N-methyl-12- phenyl-4-oxa-12- azadispiro[2.1.5.3] tridecan-8-amine 5.66 377.2 20

(5r,8r)-N-benzyl-N- methyl-12-phenyl-4- oxa-12- azadispiro[2.1.5.3] tridecan-8-amine 5.78 377.2

Example 21: (5r,8r)-8-(Methylamino)-12-ethyl-4-oxa-12-azadispiro[2.1.5.3]tridecan-13-one acetate

A mixture of example 16 (0.279 g: 081 mmol), AcOH (0.047 mL, 0.81 mmol) and palladium (30 mg, 10% wt on carbon) in MeOH (3 mL) was stirred under 3 bars of H₂ at 50° C. for 1 day. The catalyst was filtered off and the solvent was removed under vacuum to give the title compound (253 mg, 99% yield).

HPLC retention time: 1.64 min; MS: 253.2 (M+H).

This method was used for the preparation of examples 22-26 using suitable starting materials:

Ret time MS EX Structure Chemical name (min) (M + H) 22

(5s,8s)-12-ethyl-8- (methylamino)-4- oxa-12- azadispiro[2.1.5.3] tridecan-13-one acetate 1.39 253.2 23

(5s,8s)-8- (methylamino)-12- phenyl-4-oxa-12- azadispiro[2.1.5.3] tridecan-13-one acetate 2.40 301.1 24

(5r,8r)-8- (methylamino)-12- phenyl-4-oxa-12- azadispiro[2.1.5.3] tridecan-13-one acetate 2.34 301.1 25

(5s,8s)-N-methyl- 12-phenyl-4-oxa-12- azadispiro[2.1.5.3] tridecan-8-amine acetate 3.04 287.2 26

(5r,8r)-N-methyl-12- phenyl-4-oxa-12- azadispiro[2.1.5.3] tridecan-8-amine acetate 3.10 287.2

Example 27: (5r,8r)-12-Ethyl-8-[methyl(3-methylbutyl)amino]4-oxa-2-azadispiro[2.1.5.3]tridecan-13-one

A mixture of example 21 (0.253 g, 0.81 mmol), 1-bromo-3-methylbutane (0.15 mL, 0.13 mmol) and K₂CO₃ (0.56 g, 4.06 mmol) in acetonitrile (2.5 mL) was heated at 80° C. in a sealed tube overnight. 1M NaOH aqueous sol was added and it was extracted with ethyl acetate. The organic phases were combined, dried over MgSO₄, filtered and concentrated to dryness. The residue was purified by flash chromatography, C₁₈, gradient aqueous NH₄HCO₃ pH 8 to acetonitrile, to give the title compound (103 mg, 39% yield).

HPLC retention time: 3.39 min; MS: 323.2 (M+H).

This method was used for the preparation of examples 28-34 using suitable starting materials:

Ret time MS EX Structure Chemical name (min) (M + H) 28

(5s,8s)-12-ethyl-8- [methyl(3- methylbutyl)amino]- 4-oxa-12- azadispiro[2.1.5.3] tridecan-13-one 3.13 (B) 323.2 29

(5s,8s)-8-[methyl(3- methylbutyl)amino]- 12-phenyl-4-oxa-12- azadispiro[2.1.5.3] tridecan-13-one 3.79 371.2 30

(5r,8r)-8- [methyl(3- methylbutyl)amino]- 12-phenyl-4-oxa-12- azadispiro[2.1.5.3] tridecan-13-one 4.01 371.2 31

(5s,8s)-N-methyl- N-(3-methylbutyl)- 12-phenyl-4-oxa-12- azadispiro[2.1.5.3] tridecan-8-amine 4.85 357.3 32

(5r,8r)-N-methyl-N- 3-methylbutyl)-12- phenyl-4-oxa-12- azadispiro[2.1.5.3] tridecan-5-amine 4.96 357.3 33

(5s,8s)-12-ethyl-8- [methyl(2- methylpropyl) amino]-4-oxa-12- azadispiro[2.1.5.3] tridecan-13-one 3.00 (B) 309.2 34

(5r,8r)-N-methyl-12- phenyl-N-(2- phenylethyl)-4-oxa- 12- azadspiro[2.1.5.3] tridecan-8-amine 5.68 (B) 391.2

Example 35: (5r,8r)-12-Ethyl-N-methyl-N-(3-methylbutyl)-4-oxa-12-azadispiro([2.1.5.3]tridecan-8-amine

To a solution of example 27 (64 mg, 0.19 mmol) in THF (0.4 mL), borane-tetrahydrofuran complex solution (0.8 mL, 1M in THE, 0.6 mmol) was added dropwise at r.t. The reaction mixture was stirred at 65° C. for 2 h, then it was cooled to r.t. Additional borane-tetrahydrofuran complex solution (0.5 mL, 1 M in THF, 0.5 mmol) was added and it was stirred at 65° C. for 5 h. 1M NaOH aqueous sol (0.12 mL) was carefully added, cooling the mixture with an ice-water bath, and then it was heated to 70° C. for 6 h. After cooling to r.t., THF was evaporated and it was diluted with ethyl acetate. The phases were separated and the aqueous phase was back extracted with ethyl acetate. The organic phases were combined, dried over MgSO₄, filtered and concentrated to dryness. The residue was purified by flash chromatography, silica gel, gradient DCM to MeOH:DCM (1:4) to give the title compound (20 mg, 33% yield).

HPLC retention time: 3.68 min; MS: 309.2 (M+H).

Examples 36 to 40 were prepared according to the procedure described in Example 1, using suitable starting materials:

Ret time MS EX Structure Chemical name (min) (M + H) 36

(6s,9s)-9- (benzylamino)- 4-ethyl-1-oxa- 4-azaspiro[5.5] undecan-3-one 2.98 (B) 303.2 37

(6r,9r)-9- (benzylamino)- 4-ethyl-1-oxa- 4-azaspiro[5.5] undecan-3-one 3.11 (B) 303.2 38

(6s,9s)-4-ethyl- 9-(isobutyl (methyl) amino)-1-oxa- 4-azaspiro[5.5] undecan-3-one 2.46 283.2 39

(6s,9s)-9- (benzylamino)- 4-ethyl-2,2- dimethyl-1- oxa- 4-azaspiro[5.5] undecan-3-one 3.26 331.2 40

(6r,9r)-9- (benzylamino)- 4-ethyl-2,2- dimethyl-1- oxa- 4-azaspiro[5.5] undecan-3-one 3.48 331.2

Examples 41 to 44 were prepared according to the procedure described in Example 14, using suitable starting materials:

Ret Chemical time MS EX Structure name (min) (M + H) 41

(6s,9s)-9- (benzyl (methyl) amino)-4- ethyl-1-oxa-4- azaspiro[5.5] undecan-3-one 3.34 317.2 42

(6r,9r)-9- (benzyl (methyl) amino)-4- ethyl-1-oxa-4- azaspiro[5.5] undecan-3-one 3.55 317.2 43

(6s,9s)-9- (benzyl (methyl) amino)-4- ethyl-2,2- dimethyl-1- oxa-4- azaspiro[5.5] undecan-3-one 4.19 (B) 345.2 44

(6r,9r)-9- (benzyl (methyl) amino)-4- ethyl-2,2- dimethyl-1- oxa-4- azaspiro[5.5] undecan-3-one 4.31 (B) 345.2

Example 45: ((5s, 8s)-8-[Benzyl(methyl)amino]-4-oxa-12-azadispiro[2.1.5.3]tridecan-12-yl)(phenyl)methanone

Step 1. (5s,8s)-8-[Benzyl(methyl)amino]-4-oxa-12-azadispiro[2.1.5.3]tridecan-13-one. Following the methylation procedure described in Example 14, using Intermediate 5A (856 mg, 2.85 mmol) as starting material, the title compound was obtained (609 mg, 68% yield)

Step 2. (5s,8s)-N-Benzyl-N-methyl-4-oxa-12-azadispiro[2.1.5.3]tridecan-8-amine. To a solution of the product obtained in Step 1 (587 mg, 1.87 mmol) in THF (2.3 mL), LiAlH₄ solution (5.6 mL, 1 M in THF, 5.6 mmol) was added dropwise at 0-5° C. The reaction mixture was then stirred at 50° C. overnight. Additional LiAlH₄ solution (1.9 mL, 1 M in THF, 1.9 mmol) was added and it was again stirred at 50° C. overnight. 1M NaOH and ethyl acetate were carefully added and the mixture was filtered through a pad of celite. The phases were separated and the aqueous phase was back extracted with ethyl acetate. The organic phases were combined, washed with water, dried over Na₂SO₄, filtered and concentrated to dryness to give the title compound as a crude product (611 mg, overweight, quant. yield assumed).

Step 3. Title compound. To a solution of the product obtained in Step 2 (560 mg, 1.87 mmol) in DCM (6.7 mL), cooled at 0° C., benzoyl chloride (0.26 mL, 2.24 mmol) and triethylamine (0.39 mL, 2.8 mmol) were added dropwise under a nitrogen atmosphere. The reaction mixture was stirred at r.t. overnight, then NaHCO₃ sat. solution was added and it was extracted with DCM. The organic phases were combined, washed with 1M NaOH, dried over Na₂SO₄, filtered and concentrated to dryness. The residue was purified by flash chromatography, silica gel, gradient DCM to MeOH:DCM (1:4) to give the title compound (563 mg, 74% yield).

HPLC retention time (method B): 4.64 min; MS: 405.2 (M+H).

Example 46: ((5r,8r)-8-[Benzyl(methyl)amino]-4-oxa-12-azadispiro[2.1.5.3]tridecan-12-yl)(phenyl)methanone

The product was prepared according to the procedure described in Example 45, using Intermediate 5B as starting material.

HPLC retention time (method B): 4.81 min; MS: 405-2 (M+H).

Examples 47 to 50 were prepared according to the procedure described in Example 21, using suitable starting materials:

Ret time MS EX Structure Chemical name (min) (M + H) 47

(6s,9s)-4-ethyl-9- (methylamino)-1- oxa-4- azaspiro[5,5] undecan-3-one acetate 0.66 227.1 48

(6s,9s)-4-ethyl- 2,2-dimethyl-9- (methylamino)-1- oxa-4- azaspiro[5.5] undecan-3-one acetate 1.66 (B) 255.2 49

(6r,9r)-4-ethyl-2,2- dimethyl-9- (methylamino)-1- oxa-4- azaspiro[5.5] undecan-3-one acetate 1.8  (B) 255.1 50

((5s,8s)-8- (methylamino)-4- oxa-12- azadispiro[2.1.5.3] tridecan-12- yl)(phenyl) methanone acetate 2.48 (B) 315.2

Examples 51 to 60 were prepared according to the procedure described in Example 27, using suitable starting materials:

Ret time MS EX Structure Chemical name (min) (M + H) 51

(6s,9s)-4-ethyl-9- (methyl(phenethyl) amino)-1-oxa-4 azaspiro[5.5] undecan-3-one 3.34 (B) 331.2 52

(6s,9s)-4-ethyl-9- (isopentyl(methyl) amino)-1-oxa-4- azaspiro[5.5] undecan-3-one 2.82 (B) 297.2 53

(6s,9s)-4-ethyl-9- (isopentyl(methyl) amino)-2,2- dimethyl-1-oxa-4- azespiro[5.5] undecan-3-one 3.29 (B) 325.2 54

(6s,9s)-4-ethyl-9- (isobutyl(methyl) amino)-2,2- dimethyl-1-oxa-4- azaspiro[5.5] undecan-3-one 3.15 (B) 311.2 55

(6s,9s)-4-ethyl- 2,2-dimethyl-9- (methyl(phenethyl) amino)-1-oxa-4- azaspiro[5.5] undecan-3-one 3.85 (B) 359.2 56

(6r,9r)-4-ethyl-2,2- dimethyl-9- (methyl(phenethyl) amino)-1-oxa-4- azaspiro[5.5] undecan-3-one 4.06 (B) 359.2 57

(6r,9r)-4-ethyl-9- (isopentyl(methyl) amino)-2,2- dimethyl-1-oxa-4- azaspiro[5.5] undecan-3-one 3.45 (B) 325.3 58

((5s,8s)-8- [methyl(phenethyl) amino]-4-oxa-12- azadispiro[2.1.5.3] tridecan-12- yl)(phenyl) methanone 4.43 (B) 419.2 59

((5s,8s)-8- [isopentyl(methyl) amino]-4-oxa-12- azadispiro[2.1.5.3] tridecan-12- yl)(phenyl) methanone 3.94 (B) 385.2 60

((5s,8s)-8- [isobutyl(methyl) amino]-4-oxa-12- azadispiro[2.1.5.3] tridecan-12- yl)(phenyl) methanone 3.78 (B) 371.2

Examples 61 to 68 were prepared according to the procedure described in Step 2 of Example 45, using suitable starting materials:

Ret time MS EX Structure Chemical name (min) (M + H) 61

(6s,9s)-4-ethyl-N- methyl-N- phenethyl-1-oxa- 4- azaspiro[5.5] undecan-9-amine 3.68 (B) 317.2 62

(6s,9s)-N-benzyl- 4-ethyl-N,2,2- trimethyl-1-oxa-4- azaspiro[5.5] undecan-9-amine 5.84 (B) 331.2 63

(6s,9s)-4-ethyl-N- isopentyl-N- methyl-1-oxa-4- azaspiro[5.5] undecan-9-amine 3.10 (B) 283.3 64

(6s,9s)-4-ethyl-N- isopentyl-N,2,2- trimethyl-1-oxa-4- azaspiro[5.5] undecan-9-amine 4.64 (B) 311.3 65

(6s,9s)-4-ethyl-N- isobutyl-N,2,2- trimethyl-1-oxa-4- azaspiro[5.5] undecan-9-amine 4.52 (B) 297.3 66

(6s,9s)-4-ethyl- N,2,2-trimethyl-N- phenethyl-1-oxa- 4- azaspiro[5.5] undecan-9-amine 5.26 (B) 345.3 67

(5s,8s)-12-benzyl- N-methyl-N-(2- phenylethyl)-4- oxa-12- azadispiro[2.1.5.3] tridecan-8-amine 5.75 (B) 405.3 68

(5s,8s)-12-benzyl- N-isobutyl-N- methyl-4-oxa-12- azadispiro[2.1.5.3] tridecan-8-amine 5.14 (B) 357.3 Table of Examples with Binding to the σ₁-Receptor:

Biological Activity Pharmacological Study Human σ₁ Receptor Radioligand Assay

To investigate binding properties of test compounds to human σ₁ receptor, transfected HEK-293 membranes and [³H](+)-pentazocine (Perkin Elmer, NET-1056), as the radioligand, were used. The assay was carried out with 7 μg of membrane suspension, 5 nM of [³H](+)-pentazocine in either absence or presence of either buffer or 10 μM Haloperidol for total and non-specific binding, respectively. Binding buffer contained Tris-HCl 50 mM at pH 8. Plates were incubated at 37° C. for 120 minutes. After the incubation period, the reaction mix was then transferred to MultiScreen HTS, FC plates (Millipore), filtered and plates were washed 3 times with ice-cold 10 mM Tris-HCL (pH7.4). Filters were dried and counted at approximately 40% efficiency in a MicroBeta scintillation counter (Perkin-Elmer) using EcoScint liquid scintillation cocktail

Results:

As this invention is aimed at providing a compound or a chemically related series of compounds which act as ligands of the σ₁ receptor it is a very preferred embodiment in which the compounds are selected which act as ligands of the σ₁ receptor and especially compounds which have a binding expressed as K_(i) which is preferably <1000 nM, more preferably <500 nM, even more preferably <100 nM.

The following scale as been adopted for representing the binding to the the σ₁ receptor expressed as K_(i):

-   -   +K_(i)-σ₁>=500 nM     -   ++K_(i)-σ₁<500 nM     -   +++K_(i)-σ₁<100 nM

All compounds prepared in the present application exhibit binding to the σ₁ receptor, in particular the following binding results are shown:

EX K_(i)-σ₁ 1 + 2 ++ 3 +++ 4 +++ 5 +++ 6 ++ 7 +++ 8 +++ 9 ++ 10 + 11 ++ 12 + 13 + 14 ++ 15 ++ 16 +++ 17 ++ 18 ++ 19 +++ 20 +++ 21 + 22 + 23 + 24 + 25 + 26 + 27 ++ 28 ++ 29 ++ 30 +++ 31 +++ 32 +++ 33 ++ 34 +++ 35 ++ 36 + 37 + 38 ++ 39 + 40 + 41 ++ 42 +++ 43 +++ 44 ++ 45 +++ 46 ++ 47 + 48 + 49 + 50 + 51 ++ 52 ++ 53 ++ 54 ++ 55 +++ 56 +++ 57 +++ 58 ++ 59 ++ 60 ++ 61 +++ 62 +++ 63 ++ 64 +++ 65 +++ 66 +++ 67 +++ 68 +++ 

1-16. (canceled)
 17. A compound of general Formula (I):

wherein R₁ is

m is 1, 2, 3, 4 or 5; n is 0, 1, 2, 3, 4 or 5; p is 0, 1 or 2; Y is —CH₂— or —C(O)—; X is a bond, —C(R_(x)R_(x′))—, —O—, —C(O)—, —C(O)NR₇—, —NR₇C(O)— or —C(O)O—; wherein R_(x) is selected from the group consisting of halogen, —OR₇, substituted or unsubstituted C₁₋₆ alkyl, substituted or unsubstituted C₂₋₆ alkenyl and substituted or unsubstituted C₂₋₆ alkynyl; R_(x′) is selected from the group consisting of hydrogen, halogen, substituted or unsubstituted C₁₋₆ alkyl, substituted or unsubstituted C₂₋₆ alkenyl and substituted or unsubstituted C₂₋₆ alkynyl; R₇ is selected from the group consisting of hydrogen, substituted or unsubstituted C₁₋₆ alkyl, substituted or unsubstituted C₂₋₆ alkenyl and substituted or unsubstituted C₂₋₆ alkynyl; R_(1′) is selected from the group consisting of substituted or unsubstituted C₁₋₆ alkyl, substituted or unsubstituted C₂₋₆ alkenyl, substituted or unsubstituted C₂₋₆ alkynyl, substituted or unsubstituted cycloalkyl, substituted or unsubstituted aryl and substituted or unsubstituted heterocyclyl; R₂ is selected from the group consisting of hydrogen, substituted or unsubstituted C₁₋₆ alkyl, substituted or unsubstituted C₂₋₆ alkenyl, substituted or unsubstituted C₂₋₆ alkynyl, substituted or unsubstituted cycloalkyl, substituted or unsubstituted aryl and substituted or unsubstituted heterocyclyl; R₃ and R_(3′) are independently selected from the group consisting of hydrogen, substituted or unsubstituted C₁₋₆ alkyl, substituted or unsubstituted C₂₋₆ alkenyl, substituted or unsubstituted C₂₋₆ alkynyl, substituted or unsubstituted cycloalkyl, substituted or unsubstituted alkylcycloalkyl, substituted or unsubstituted alkylaryl, substituted or unsubstituted aryl, substituted or unsubstituted heterocyclyl or substituted or unsubstituted alkylheterocyclyl; or R₃ and R_(3′), together with the carbon atom to which they are attached, form a substituted or unsubstituted cycloalkyl; R₄ and R_(4′) are independently selected from the group consisting of hydrogen, substituted or unsubstituted C₁₋₆ alkyl, substituted or unsubstituted C₂₋₆ alkenyl and substituted or unsubstituted C₂₋₆ alkynyl; R₅ and R_(5′) are independently selected from the group consisting of hydrogen, substituted or unsubstituted C₁₋₆ alkyl, substituted or unsubstituted C₂₋₆ alkenyl and substituted or unsubstituted C₂₋₆ alkynyl; or R₅ and R_(5′) together with the carbon atom to which they are attached, form a substituted or unsubstituted cycloalkyl or a substituted or unsubstituted heterocyclyl; R₆ and R_(6′) are independently selected from the group consisting of hydrogen, halogen, substituted or unsubstituted C₁₋₆ alkyl, substituted or unsubstituted C₂₋₆ alkenyl, substituted or unsubstituted C₂₋₆ alkynyl, —CHOR₈ and —C(O)OR₈; wherein R₈ is selected from the group consisting of hydrogen, substituted or unsubstituted C₁₋₆ alkyl, substituted or unsubstituted C₂₋₆ alkenyl and substituted or unsubstituted C₂₋₆ alkynyl; R_(n) is selected from the group consisting of hydrogen, unsubstituted C₁₋₆ alkyl, unsubstituted C₂₋₆ alkenyl and unsubstituted C₂₋₆ alkynyl; optionally as a stereoisomer, including enantiomers and diastereomers, a racemate or a mixture of at least two stereoisomers, including enantiomers and/or diastereomrers, in any mixing ratio, or a corresponding salt thereof, or a corresponding solvate thereof; with the proviso that when Y is —C(O)—; then R₁ is not


18. The compound according to claim 17, wherein X is a bond.
 19. The compound according to claim 17, wherein R_(1′) is selected from the group consisting of substituted or unsubstituted C₁₋₆ alkyl, substituted or unsubstituted C₂₋₆ alkenyl, substituted or unsubstituted C₂₋₆ alkynyl, substituted or unsubstituted cycloalkyl, substituted or unsubstituted aryl and substituted or unsubstituted heterocyclyl.
 20. The compound according to claim 19, wherein R_(1′) is substituted or unsubstituted methyl, substituted or unsubstituted ethyl or substituted or unsubstituted phenyl.
 21. The compound according to claim 17, wherein R₂ is selected from the group consisting of hydrogen, substituted or unsubstituted C₁₋₆ alkyl, substituted or unsubstituted C₂₋₆ alkenyl, substituted or unsubstituted C₂₋₆ alkynyl, substituted or unsubstituted cycloalkyl, substituted or unsubstituted aryl and substituted or unsubstituted heterocyclyl.
 22. The compound according to claim 21, wherein R₂ is hydrogen, substituted or unsubstituted isopropyl, substituted or unsubstituted isobutyl or substituted or unsubstituted phenyl.
 23. The compound according to claim 17, wherein R₃ and R_(3′), together with the carbon atom to which they are attached, form a substituted or unsubstituted cycloalkyl.
 24. The compound according to claim 23, wherein R₃ and R_(3′) form a substituted or unsubstituted cyclopropyl.
 25. The compound according to claim 17, which is a compound of Formula (I′)


26. The compound according to claim 17, which is a compound of Formula (I^(2′))


27. The compound according to claim 17, which is a compound of Formula (I^(3′))


28. The compound according to claim 17, which is selected from the group consisting of: (5s,8s)-8-(benzylamino)-12-ethyl-4-oxa-12-azadispiro[2.1.5.3]tridecan-13-one, (5r,8r)-8-(benzylamino)-12-ethyl-4-oxa-12-azadispiro[2.1.5.3]tridecan-13-one, (5s,8s)-12-ethyl-8-[methyl(2-phenylethyl)amino]-4-oxa-12-azadispiro[2.1.5.3]tridecan-13-one, (5r,8r)-12-ethyl-8-[methyl(2-phenylethyl)amino]-4-oxa-12-azadispiro[2.1.5.3]tridecan-13-one, (5s,8s)-8-[benzyl(methyl)amino]-12-ethyl-4-oxa-12-azadispiro[2.1.5.3]tridecan-13-one, (5s,8s)-12-ethyl-8-[(2-phenylethyl)amino]-4-oxa-12-azadispiro[2.1.5.3]tridecan-13-one, (5r,8r)-12-ethyl-8-[(2-phenylethyl)amino]-4-oxa-12-azadispiro[2.1.5.3]tridecan-13-one, (5s,8s)-8-[benzyl(methyl)amino]-12-phenyl-4-oxa-12-azadispiro[2.1.5.3]tridecan-13-one, (5s,8s)-8-[methyl(2-phenylethyl)amino]-12-phenyl-4-oxa-12-azadispiro[2.1.5.3]tridecan-13-one, (5s,8s)-8-(benzylamino)-12-phenyl-4-oxa-12-azadispiro[2.1.5.3]tridecan-13-one, (5s,8s)-12-phenyl-8-[(2-phenylethyl)amino]-4-oxa-12-azadispiro[2.1.5.3]tridecan-13-one, (5r,8r)-8-(benzylamino)-12-phenyl-4-oxa-12-azadispiro[2.1.5.3]tridecan-13-one, (5r,8r)-12-phenyl-8-[(2-phenylethy)amino]-4-oxa-12-azadispiro[2.1.5.3]tridecan-13-one, (5r,8r)-8-[benzyl(methyl)amino]-12-phenyl-4-oxa-12-azadispiro[2.1.5.3]tridecan-13-one, (5r,8r)-8-[methyl(2-phenylethyl)amino]-12-phenyl-4-oxa-12-azadispiro[2.1.5.3]tridecan-13-one, (5r,8r)-8-[benzyl(methyl)amino]-12-ethyl-4-oxa-12-azadispiro[2.1.5.3]tridecan-13-one, (5s,8s)-N-benzyl-12-ethyl-N-methyl-4-oxa-12-azadispiro[2.1.5.3]tridecan-8-amine, (5r,8r)-N-benzyl-12-ethyl-N-methyl-4-oxa-12-azadispiro[2.1.5.3]tridecan-8-amine, (5s, 8s)-N-benzyl-N-methyl-12-phenyl-4-oxa-12-azadispiro[2.1.5.3]tridecan-8-amine (5r,8r)-N-benzyl-N-methyl-12-phenyl-4-oxa-12-azadispiro[2.1.5.3]tridecan-8-amine, (5r,8r)-12-ethyl-8-(methylamino)-4-oxa-12-azadispiro[2.1.5.3]tridecan-13-one acetate, (5s,8s)-12-ethyl-8-(methylamino)-4-oxa-12-azadispiro[2.1.5.3]tridecan-13-one acetate, (5s,8s)-8-(methylamino)-12-phenyl-4-oxa-12-azadispiro[2.1.5.3]tridecan-13-one acetate, (5r,8r)-8-(methylamino)-12-phenyl-4-oxa-12-azadispiro[2.1.5.3]tridecan-13-one acetate, (5s,8s)-N-methyl-12-phenyl-4-oxa-12-azadispiro[2.1.5.3]tridecan-8-amine acetate, (5r,8r)-N-methyl-12-phenyl-4-oxa-12-azadispiro[2.1.5.3]tridecan-8-amine acetate, (5r,8r)-12-ethyl-8-[methyl(3-methylbutyl)amino]-4-oxa-12-azadispiro[2.1.5.3]tridecan-13-one, (5s,8s)-12-ethyl-8-[methyl(3-methylbutyl)amino]-4-oxa-12-azadispiro[2.1.5.3]tridecan-13-one, (5s,8s)-8-[methyl(3-methylbutyl)amino]-12-phenyl-4-oxa-12-azadispiro[2.1.5.3]tridecan-13-one, (5r,8r)-8-[methyl(3-methylbutyl)amino]-12-phenyl-4-oxa-12-azadispiro[2.1.5.3]tridecan-13-one, (5s,8s)-N-methyl-N-(3-methylbutyl)-12-phenyl-4-oxa-12-azadispiro[2.1.5.3]tridecan-8-amine, (5r,8r)-N-methyl-N-(3-methylbutyl)-12-phenyl-4-oxa-12-azadispiro[2.1.5.3]tridecan-8-amine, (5s,8s)-12-ethyl-8-[methyl(2-methylpropyl)amino]-4-oxa-12-azadispiro[2.1.5.3]tridecan-13-one, (5r,8r)-N-methyl-12-phenyl-N-(2-phenylethyl)-4-oxa-12-azadispiro[2.1.5.3]tridecan-8-amine and (5r,8r)-12-ethyl-N-methyl-N-(3-methylbutyl)-4-oxa-12-azadispiro[2.1.5.3]tridecan-8-amine.
 29. The compound according to claim 17, which is selected from the group consisting of: (6s,9s)-9-(benzylamino)-4-ethyl-1-oxa-4-azaspiro[5.5]undecan-3-one, (6r,9r)-9-(benzylamino)-4-ethyl-1-oxa-4-azaspiro[5.5]undecan-3-one, (6s,9s)-4-ethyl-9-(isobutyl(methyl)amino)-1-oxa-4-azaspiro[5.5]undecan-3-one, (6s,9s)-9-(benzylamino)-4-ethyl-2,2-dimethyl-1-oxa-4-azaspiro[5.5]undecan-3-one, (6r,9r)-9-(benzylamino)-4-ethyl-2,2-dimethyl-oxa-4-azaspiro[5.5]undecan-3-one, (6s,9s)-9-(benzyl(methyl)amino)-4-ethyl-1-oxa-4-azaspiro[5.5]undecan-3-one, (6r,9r)-9-(benzyl(methyl)amino)-4-ethyl-oxa-4-azaspiro[5.5]undecan-3-one, (6s,9s)-9-(benzyl(methy)amino)-4-ethyl-2,2-dimethyl-1-oxa-4-azaspiro[5.5]undecan-3-one, (6r,9r)-9-(benzyl(methyl)amino)-4-ethyl-2,2-dimethyl-1-oxa-4-azaspiro[5.5]undecan-3-one, ((5s,8s)-8-[Benzyl(methyl)amino]-4-oxa-12-azadispiro[2.1.5.3]tridecan-12-yl)(phenyl)methanone, ((5r,8r)-8-[Benzyl(methyl)amino]-4-oxa-12-azadispiro[2.1.5.3]tridecan-12-yl)(phenyl)methanone, (6s,9s)-4-ethyl-9-(methylamino)-1-oxa-4-azaspiro[5.5]undecan-3-one acetate, (6s,9s)-4-ethyl-2,2-dimethyl-9-(methylamino)-1-oxa-4-azaspiro[5.5]undecan-3-one acetate, (6r,9r)-4-ethyl-2,2-dimethyl-9-(methylamino)-1-oxa-4-azaspiro[5.5]undecan-3-one acetate, ((5s,8s)-8-(methylamino)-4-oxa-12-azadispiro[2.1.5.3]tridecan-12-yl)(phenyl)methanone acetate, (6s,9s)-4-ethyl-9-(methyl(phenethyl)amino)-1-oxa-4-azaspiro[5.5]undecan-3-one, (6s,9s)-4-ethyl-9-(isopentyl(methyl)amino)-1-oxa-4-azaspiro[5.5]undecan-3-one, (6s,9s)-4-ethyl-9-(isopentyl(methyl)amino)-2,2-dimethyl-1-oxa-4-azaspiro[5.5]undecan-3-one, (6s,9s)-4-ethyl-9-(isobutyl(methyl)amino)-2,2-dimethyl-1-oxa-4-azaspiro[5.5]undecan-3-one, (6s,9s)-4-ethyl-2,2-dimethyl-9-(methyl(phenethyl)amino)-1-oxa-4-azaspiro[5.5]undecan-3-one, (6r,9r)-4-ethyl-2,2-dimethyl-9-(methyl(phenethyl)amino)-1-oxa-4-azaspiro[5.5]undecan-3-one, (6r,9r)-4-ethyl-9-(isopentyl(methyl)amino)-2,2-dimethyl-1-oxa-4-azaspiro[5.5]undecan-3-one, ((5s,8s)-8-[methyl(phenethyl)amino]-4-oxa-12-azadispiro[2.1.5.3]tridecan-12-yl)(phenyl)methanone, ((5s,8s)-8-[isopentyl(methyl)amino]-4-oxa-12-azadispiro[2.1.5.3]tridecan-12-yl)(phenyl)methanone, ((5s,8s)-8-[isobutyl(methyl)amino]-4-oxa-12-azadispiro[2.1.5.3]tridecan-12-yl)(phenyl)methanone, (6s,9s)-4-ethyl-N-methyl-N-phenethyl-1-oxa-4-azaspiro[5.5]undecan-9-amine, (6s,9s)-N-benzyl-4-ethyl-N,2,2-trimethyl-1-oxa-4-azaspiro[5.5]undecan-9-amine, (6s,9s)-4-ethyl-N-isopentyl-N-methyl-1-oxa-4-azaspiro[5.5]undecan-9-amine, (6s,9s)-4-ethyl-N-isopentyl-N,2,2-trimethyl-1-oxa-4-azaspiro[5.5]undecan-9-amine, (6s,9s)-4-ethyl-N-isobutyl-N,2,2-trimethyl-1-oxa-4-azaspiro[5.5]undecan-9-amine, (6s,9s)-4-ethyl-N,2,2-trimethyl-N-phenethyl-1-oxa-4-azaspiro[5.5]undecan-9-amine, (5s,8s)-12-benzyl-N-methyl-N-(2-phenylethyl)-4-oxa-12-azadispiro[2.1.5.3]tridecan-8-amine and (5s,8s)-12-benzyl-N-isobutyl-N-methyl-4-oxa-12-azadispiro[2.1.5.3]tridecan-8-amine.
 30. A process for the preparation of the compound according to claim 17, wherein when R₁ is —(CR₄R_(4′))_(p)R_(1′), which process comprises: a) the intramolecular cyclization of a compound of formula VII

or b) the reaction of a compound of formula XI

with a compound of formula XVI

or c) the incorporation of the group —N(R_(n))(CR₅R_(5′))_(m)X(CR₆R_(6′))_(n)R₂ by reaction of a ketone of formula VIIIK

with an amine of formula XVII

wherein R₁, R_(1′), R₂, R₃, R_(3′), R₄, R_(4′), R₅, R_(5′), R₆, R_(6′), R₇, R₈, R_(n), R_(x), R_(x′), m, n, p, X and Y have the meanings as defined in claim 17 for the compound of Formula (I), LG represents a leaving group, including halogen, mesylate, tosylate and triflate, with the proviso that when Y═CO, LG represents chloro or bromo, and V represents an aldehyde or a leaving group, including halogen, mesylate, tosylate and triflate.
 31. A process for the preparation of the compound according to claim 17, wherein Y is CH₂ and R₁ is —C(O)—R_(1′), which process comprises: reacting a compound of formula XXXIV

with an acylating agent of formula XXXVI

wherein R_(1′), R₂, R₃, R_(3′), R₅, R_(5′), R₆, R_(6′), R₇, R₈, R_(n), R_(x), R_(x′), m, n and X have the meanings as defined in claim 17 for the compound of Formula (I), and Z represents OH or halogen, including bromo and chloro.
 32. A process for the preparation of the compound of Formula (I) according to claim 17, employing a compound of Formula II, IIP, III, IIIP, XIII, XIIIP, XII, IV, V, VP, VI, XIV, XIVP, X, XP, VII, VIIP, XV, XVP, XVK, XI, XIP, XIK, XVI, VIIIP, VIIIK, XVII, Ie, XXIP, XXIK, XXII, XVIIIP, XVIIIK, Ic, XIX, XIXP, XXP, XXK, XXIV, XXIVP, XXIVK, XXVI, XXVIP, XXVIK, XXIIIP, XXIIIK, Ig, XXVP, XXVK, Ih, XXVIIP, XXVIIK, XXVIIIa, XXIXP, XXIXK, XXVIIIb, XXXP, XXXK, XXVIIIc, XVIIIP, XVIIIK, XVII, Im, XXXIIIP, XXXIIIK, In, XXXVP, XXXVK, XXXII, XXXIIP, XXXIIK, XXXIV, XXXIVP, XXXVI, XXXVIIP, XXXVIIK, XXXP, XXXK, XXXIP, XXXIK or XVII

wherein R₁, R_(1′), R₂, R₃, R_(3′), R₄, R_(4′), R₅, R_(5′), R₆, R_(6′), R₇, R₈, R_(n), R_(x), R_(x′), m, n, p, X and Y have the meanings as defined in claim 17 for the compound of Formula (I), LG represents a leaving group, including halogen, mesylate, tosylate and triflate, with the proviso that when Y═CO, LG represents chloro or bromo, P′ represents a suitable protecting group, including 4-methoxybenzyl and benzyl, Q represents methyl or benzyl, and Z represents OH or halogen, including bromo and chloro.
 33. A pharmaceutical composition which comprises the compound according to claim 17, or a pharmaceutically acceptable salt thereof, and a pharmaceutically acceptable carrier, adjuvant or vehicle.
 34. A method of treating pain in a subject in need thereof, comprising administration of an effective amount of the compound according to claim
 17. 35. The method according to claim 34, wherein the pain is selected from the group consisting of medium to severe pain, visceral pain, chronic pain, cancer pain, migraine, inflammatory pain, acute pain, neuropathic pain, allodynia and hyperalgesia. 